Canonical Allele Identifier: PA916019383
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 41212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Gly274Ala
CA344205
NM_001302960.2:c.821G>C