Allele Registry

Canonical Allele Identifier: PA3057632937

Gene: CYP2C19 HGNC NCBI

ClinVar RCV:

RCV005320712

ClinVar Variation:

3837856

HGVS (amino-acid)	Matching Registered Transcripts
NP_000760.1:p.Cys164Phe	CA377670430 NM_000769.4:c.491G>T