Canonical Allele Identifier: PA658814939
Gene: HSD3B7 HGNC NCBI

Linked Data

ClinVar Variation Id: 502643
ClinVar RCV Id: RCV000595257 RCV004024860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079469.2:p.Val224Ala
CA8018071
NM_025193.4:c.671T>C