Canonical Allele Identifier: PA2826875428
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1753434
ClinVar RCV Id: RCV002361677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Met155Arg
CA381551368
NM_001302959.2:c.464T>G