Canonical Allele Identifier: PA2829915793
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2887708
ClinVar RCV Id: RCV003619511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064693.2:p.Arg1082Ser
CA384118244
NM_020297.3:c.3246G>T
CA384118245
NM_020297.3:c.3246G>C