Canonical Allele Identifier: PA2828705123
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1786499
ClinVar RCV Id: RCV002430464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Ser713Pro
CA384132722
NM_001377273.1:c.2137T>C