Canonical Allele Identifier: PA2827397828
Gene: CYP19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 990912
ClinVar RCV Id: RCV001279030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334179.1:p.Ala165Thr
CA7560041
NM_001347250.2:c.493G>A