Canonical Allele Identifier: PA2825501713
Gene: CYP11A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17523
ClinVar RCV Id: RCV000019075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093243.1:p.Val257Glu
CA127241
NM_001099773.2:c.770T>A