Canonical Allele Identifier: PA2826875477
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 41197
ClinVar RCV Id: RCV000034096 RCV004018729 RCV001379496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Cys179Tyr
CA344155
NM_001302959.2:c.536G>A