Canonical Allele Identifier: PA2580470392
Gene: HSD3B7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2191305
ClinVar RCV Id: RCV002616841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079469.2:p.Arg282Trp
CA8018124
NM_025193.4:c.844C>T