Canonical Allele Identifier: PA2827397609
Gene: CYP19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17826
ClinVar RCV Id: RCV000019404 RCV001851942
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334178.1:p.Glu210Lys
CA127462
NM_001347249.1:c.628G>A