Canonical Allele Identifier: PA2828705126
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 45400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Ala717Thr
CA136256
NM_001377273.1:c.2149G>A