Canonical Allele Identifier: PA2828705381
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2887708
ClinVar RCV Id: RCV003619511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Arg1082Ser
CA384118244
NM_001377273.1:c.3246G>T
CA384118245
NM_001377273.1:c.3246G>C