Allele Registry

Canonical Allele Identifier: PA127459

Gene: CYP19A1 HGNC NCBI

ClinVar RCV:

RCV000019396

ClinVar Variation:

17818

HGVS (amino-acid)	Matching Registered Transcripts
NP_112503.1:p.Arg375Cys	CA127458 NM_031226.3:c.1123C>T