Canonical Allele Identifier: PA913198640
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 623799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Ser1520Cys
CA384129332
NM_005691.3:c.4559C>G