Canonical Allele Identifier: PA2827398601
Gene: CYP19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334182.1:p.Glu210Lys
CA127462
NM_001347253.2:c.628G>A