Allele Registry

Canonical Allele Identifier: PA101578

Gene: CYP19A1 HGNC NCBI

ClinVar RCV:

RCV000019396

ClinVar Variation:

17818

HGVS (amino-acid)	Matching Registered Transcripts
NP_000094.2:p.Arg375Cys	CA127458 NM_000103.4:c.1123C>T