Canonical Allele Identifier: PA2828704835
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 848709
ClinVar RCV Id: RCV001052526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Lys274Thr
CA384122197
NM_001377273.1:c.821A>C