Canonical Allele Identifier: PA136301
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 45416
ClinVar RCV Id: RCV000038619 RCV000618677 RCV001038743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Arg1506Cys
CA136299
NM_005691.3:c.4516C>T