Allele Registry

Canonical Allele Identifier: PA2827398167

Gene: CYP19A1 HGNC NCBI

ClinVar RCV:

RCV000019396

ClinVar Variation:

17818

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334180.1:p.Arg375Cys	CA127458 NM_001347251.2:c.1123C>T