Canonical Allele Identifier: PA2580470388
Gene: HSD3B7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2405171
ClinVar RCV Id: RCV002759393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079469.2:p.Ala219Val
CA8018064
NM_025193.4:c.656C>T