Canonical Allele Identifier: PA2826875347
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2675313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Lys116Gln
CA381550580
NM_001302959.2:c.346A>C