Canonical Allele Identifier: PA2827398904
Gene: CYP19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17821
ClinVar RCV Id: RCV000019399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334183.1:p.Arg365Gln
CA127460
NM_001347254.2:c.1094G>A