Canonical Allele Identifier: PA105586
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 856369
ClinVar RCV Id: RCV001061813 RCV001311294 RCV002479365 RCV003307898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Ala1513Thr
CA6480818
NM_005691.3:c.4537G>A