Canonical Allele Identifier: PA2827397465
Gene: CYP19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334177.1:p.Arg435Cys
CA127454
NM_001347248.1:c.1303C>T