Canonical Allele Identifier: PA2825848489
Gene: HSD3B7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3107182
ClinVar RCV Id: RCV004404536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136249.1:p.Phe123Leu
CA8017980
NM_001142777.2:c.367T>C
CA395639978
NM_001142777.2:c.369C>A
CA395639980
NM_001142777.2:c.369C>G