Canonical Allele Identifier: PA136260
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 45400
ClinVar RCV Id: RCV000038597 RCV001046473
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064693.2:p.Ala717Thr
CA136256
NM_020297.3:c.2149G>A