Allele Registry

Canonical Allele Identifier: PA2827398307

Gene: CYP19A1 HGNC NCBI

ClinVar RCV:

RCV000414127

ClinVar Variation:

373729

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334181.1:p.Met127Thr	CA16042890 NM_001347252.2:c.380T>C