Canonical Allele Identifier: PA645417708
Gene: HSD3B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 292255
ClinVar RCV Id: RCV000391205 RCV000941557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159592.1:p.Cys5Ser
CA1035859
NM_001166120.2:c.13T>A
CA341394030
NM_001166120.2:c.14G>C