Allele Registry

Canonical Allele Identifier: PA2499234128

Gene: CYP2C9 HGNC NCBI

ClinVar RCV:

RCV001516506

ClinVar Variation:

1167372

HGVS (amino-acid)	Matching Registered Transcripts
NP_000762.2:p.Arg125His	CA5617037 NM_000771.4:c.374G>A