Canonical Allele Identifier: PA2826875582
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1394137
ClinVar RCV Id: RCV001898451 RCV002449544
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289888.1:p.Ala227Val
CA6140992
NM_001302959.2:c.680C>T