Canonical Allele Identifier: PA2828704982
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2771182
ClinVar RCV Id: RCV003510416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Leu526Pro
CA384139093
NM_001377273.1:c.1577T>C