Allele Registry

Canonical Allele Identifier: PA290561

Gene: CYP19A1 HGNC NCBI

ClinVar RCV:

RCV000124653

RCV000278064

RCV001522786

ClinVar Variation:

137064

HGVS (amino-acid)	Matching Registered Transcripts
NP_112503.1:p.Arg264Cys	CA290560 NM_031226.3:c.790C>T