Canonical Allele Identifier: PA2827398967
Gene: CYP19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 316471
ClinVar RCV Id: RCV000264992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334183.1:p.Val460Met
CA7559791
NM_001347254.2:c.1378G>A