Canonical Allele Identifier: PA2826875249
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 821607
ClinVar RCV Id: RCV001016168 RCV003736957
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Phe29Cys
CA6140757
NM_001302959.2:c.86T>G