Canonical Allele Identifier: PA2826876227
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1928982
ClinVar RCV Id: RCV002642266 RCV003289564
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Glu246Asp
CA381551832
NM_001302960.2:c.738G>T
CA381551833
NM_001302960.2:c.738G>C