Canonical Allele Identifier: PA119593
Gene: CYP2C9 HGNC NCBI

Linked Data

ClinVar Variation Id: 8409
ClinVar RCV Id: RCV000008920 RCV000309101 RCV000723560 RCV000788099 RCV000787929 RCV000788093 RCV001263463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000762.2:p.Arg144Cys
CA119592
NM_000771.4:c.430C>T
CA356589
NM_000771.4:c.[430C>T;1075A=]