Allele Registry

Canonical Allele Identifier: PA2827398501

Gene: CYP19A1 HGNC NCBI

ClinVar RCV:

RCV000344503

RCV002061186

RCV003930364

ClinVar Variation:

316480

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334182.1:p.Val17Met	CA7560176 NM_001347253.2:c.49G>A