Canonical Allele Identifier: PA913200102
Gene: HSD3B7 HGNC NCBI

Linked Data

ClinVar Variation Id: 594920
ClinVar RCV Id: RCV000730322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079469.2:p.Leu189Phe
CA395641222
NM_025193.4:c.565C>T