Canonical Allele Identifier: PA2827397962
Gene: CYP19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17816
ClinVar RCV Id: RCV000019394
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334179.1:p.Cys437Tyr
CA127456
NM_001347250.2:c.1310G>A