Canonical Allele Identifier: PA2825079973
Gene: HSD3B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2674656
ClinVar RCV Id: RCV003459900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000189.1:p.Val116Gly
CA341396013
NM_000198.4:c.347T>G