Allele Registry

Canonical Allele Identifier: PA2827398369

Gene: CYP19A1 HGNC NCBI

ClinVar RCV:

RCV000124653

RCV000278064

RCV001522786

ClinVar Variation:

137064

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334181.1:p.Arg264Cys	CA290560 NM_001347252.2:c.790C>T