Canonical Allele Identifier: PA1139736874
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_064693.2:p.Lys274Thr
CA384122197
NM_020297.3:c.821A>C