Canonical Allele Identifier: PA2828704968
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1377020
ClinVar RCV Id: RCV001889806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Ile498Val
CA384139438
NM_001377273.1:c.1492A>G