Canonical Allele Identifier: PA2829621590
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2887708
ClinVar RCV Id: RCV003619511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Arg1082Ser
CA384118244
NM_005691.3:c.3246G>T
CA384118245
NM_005691.3:c.3246G>C