Canonical Allele Identifier: PA645461747
Gene: HSD3B7 HGNC NCBI

Linked Data

ClinVar Variation Id: 261875
ClinVar RCV Id: RCV000243230 RCV000967411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079469.2:p.Ala286Thr
CA8018129
NM_025193.4:c.856G>A