Canonical Allele Identifier: PA2829622475
Gene: ABCC9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1021093
ClinVar RCV Id: RCV001320789 RCV002499623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005682.2:p.Ter1550Tyr
CA384128568
NM_005691.3:c.4650G>T
CA384128572
NM_005691.3:c.4650G>C