Canonical Allele Identifier: PA121928
Gene: HSD3B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12188
ClinVar RCV Id: RCV000012971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159592.1:p.Ala10Glu
CA121927
NM_001166120.2:c.29C>A