Allele Registry

Canonical Allele Identifier: PA915965183

Gene: CYP2C19 HGNC NCBI

ClinVar RCV:

RCV000948522

ClinVar Variation:

39354

HGVS (amino-acid)	Matching Registered Transcripts
NP_000760.1:p.Ile331Val	CA211687318 NM_000769.4:c.991A>G CA918736669 NM_000769.4:c.990_991delinsTG