Allele Registry

Canonical Allele Identifier: PA2827398705

Gene: CYP19A1 HGNC NCBI

ClinVar RCV:

RCV000019393

RCV000814400

ClinVar Variation:

17815

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334182.1:p.Arg435Cys	CA127454 NM_001347253.2:c.1303C>T