Canonical Allele Identifier: PA2828705368
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1507972
ClinVar RCV Id: RCV002040296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364202.1:p.Met1060Thr
CA384118568
NM_001377273.1:c.3179T>C