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See variants in ClinVar
See Variation Viewer (GRCh37.p13)
See Variation Viewer (GRCh38)
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These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.
NM_001477.1 → NP_001468.1 G antigen 12I
See identical proteins and their annotated locations for NP_001468.1
Status: REVIEWED
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