Canonical Allele Identifier: PA2827397757
Gene: CYP19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 316480
ClinVar RCV Id: RCV000344503 RCV002061186 RCV003930364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334179.1:p.Val17Met
CA7560176
NM_001347250.2:c.49G>A