Canonical Allele Identifier: PA2829477424
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1717805
ClinVar RCV Id: RCV002297814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Gly117Asp
CA381549222
NM_003977.4:c.350G>A