Allele Registry

Canonical Allele Identifier: PA2827399008

Gene: CYP19A1 HGNC NCBI

ClinVar RCV:

RCV000310608

RCV000881105

RCV002139473

ClinVar Variation:

316479

1606711

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334184.1:p.Trp39Arg	CA7560164 NM_001347255.2:c.115T>C CA392422972 NM_001347255.2:c.115T>A