Canonical Allele Identifier: PA645461650
Gene: HSD3B7 HGNC NCBI

Linked Data

ClinVar Variation Id: 391606
ClinVar RCV Id: RCV000437971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079469.2:p.Ser129Gly
CA16607411
NM_025193.4:c.385A>G