Canonical Allele Identifier: PA2829620415
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1775942
ClinVar RCV Id: RCV002398459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Thr531Ser
CA233633317
NM_005691.3:c.1592C>G
CA384139040
NM_005691.3:c.1591A>T