Canonical Allele Identifier: PA351877
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 222474
ClinVar RCV Id: RCV000208244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Arg1095His
CA351874
NM_005691.3:c.3284G>A