Canonical Allele Identifier: PA2499271689
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000587
ClinVar RCV Id: RCV001296739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Leu1515Arg
CA6480817
NM_005691.3:c.4544T>G