Canonical Allele Identifier: PA1139748484
Gene: CYP19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 990912
ClinVar RCV Id: RCV001279030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112503.1:p.Ala165Thr
CA7560041
NM_031226.3:c.493G>A