Canonical Allele Identifier: PA2828705889
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 45400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364203.1:p.Ala429Thr
CA136256
NM_001377274.1:c.1285G>A