Canonical Allele Identifier: PA2826875901
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 821721
ClinVar RCV Id: RCV001016414
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289889.1:p.Asp91Gly
CA381547412
NM_001302960.2:c.272A>G