Canonical Allele Identifier: PA915998105
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 821721
ClinVar RCV Id: RCV001016414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Asp91Gly
CA381547412
NM_003977.4:c.272A>G