Allele Registry

Canonical Allele Identifier: PA2827397416

Gene: CYP19A1 HGNC NCBI

ClinVar RCV:

RCV000019399

ClinVar Variation:

17821

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334177.1:p.Arg365Gln	CA127460 NM_001347248.1:c.1094G>A