Canonical Allele Identifier: PA2825080233
Gene: HSD3B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 487802
ClinVar RCV Id: RCV000577852

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000189.1:p.Arg335Gln
CA30212310
NM_000198.4:c.1004G>A