Canonical Allele Identifier: PA136238
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 45395
ClinVar RCV Id: RCV000038592 RCV000767084 RCV000988800 RCV001256792 RCV002490525 RCV004018877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Arg663Cys
CA136235
NM_005691.3:c.1987C>T