Canonical Allele Identifier: PA2825848477
Gene: HSD3B7 HGNC NCBI

Linked Data

ClinVar Variation Id: 593982
ClinVar RCV Id: RCV000729172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136249.1:p.Gly88Ala
CA395639519
NM_001142777.2:c.263G>C