Allele Registry

Canonical Allele Identifier: PA2827398662

Gene: CYP19A1 HGNC NCBI

ClinVar Allele:

32857

ClinVar RCV:

RCV000019396

ClinVar Variation:

17818

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334182.1:p.Arg375Cys	CA127458 NM_001347253.2:c.1123C>T