Canonical Allele Identifier: PA2825848474
Gene: HSD3B7 HGNC NCBI

Linked Data

ClinVar Variation Id: 596758
ClinVar RCV Id: RCV000732692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136249.1:p.Ala76Pro
CA395639444
NM_001142777.2:c.226G>C