Canonical Allele Identifier: PA2826875254
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 821721
ClinVar RCV Id: RCV001016414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Asp32Gly
CA381547412
NM_001302959.2:c.95A>G