Allele Registry

Canonical Allele Identifier: PA2827397355

Gene: CYP19A1 HGNC NCBI

ClinVar Allele:

332373

ClinVar RCV:

RCV000293196

RCV001520086

RCV001529832

ClinVar Variation:

316476

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334177.1:p.Thr201Met	CA7560016 NM_001347248.1:c.602C>T