Allele Registry

Canonical Allele Identifier: PA2827397962

Gene: CYP19A1 HGNC NCBI

ClinVar RCV:

RCV000019394

ClinVar Variation:

17816

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334179.1:p.Cys437Tyr	CA127456 NM_001347250.2:c.1310G>A