Allele Registry

Canonical Allele Identifier: PA2825068838

Gene: CYP19A1 HGNC NCBI

ClinVar Variation Id: 316480

HGVS (amino-acid)	Matching Registered Transcripts
NP_000094.2:p.Val17Met	CA7560176 NM_000103.4:c.49G>A