Canonical Allele Identifier: PA2828705431
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 31946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Arg1154Trp
CA260058
NM_001377273.1:c.3460C>T