Allele Registry

Canonical Allele Identifier: PA101587

Gene: CYP19A1 HGNC NCBI

ClinVar RCV:

RCV000019393

RCV000814400

ClinVar Variation:

17815

HGVS (amino-acid)	Matching Registered Transcripts
NP_000094.2:p.Arg435Cys	CA127454 NM_000103.4:c.1303C>T