Canonical Allele Identifier: PA2826875564
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 827554
ClinVar RCV Id: RCV001027357 RCV001042436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Ala217Gly
CA381554619
NM_001302959.2:c.650C>G