Canonical Allele Identifier: PA2827397466
Gene: CYP19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17816
ClinVar RCV Id: RCV000019394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334177.1:p.Cys437Tyr
CA127456
NM_001347248.1:c.1310G>A