Canonical Allele Identifier: PA2829477885
Gene: AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1034759
ClinVar RCV Id: RCV001337527 RCV002412053
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003968.3:p.Ala286Thr
CA381554886
NM_003977.4:c.856G>A