Canonical Allele Identifier: PA2827398572
Gene: CYP19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 990912
ClinVar RCV Id: RCV001279030
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334182.1:p.Ala165Thr
CA7560041
NM_001347253.2:c.493G>A