Canonical Allele Identifier: PA658814925
Gene: HSD3B7 HGNC NCBI

Linked Data

ClinVar Variation Id: 499368
ClinVar RCV Id: RCV000592050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079469.2:p.Thr86Met
CA8017938
NM_025193.4:c.257C>T