Canonical Allele Identifier: PA095352
Gene: HSD17B10 HGNC NCBI

Linked Data

ClinVar Variation Id: 11442
ClinVar RCV Id: RCV000012195 RCV001224055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004484.1:p.Arg130Cys
CA121447
NM_004493.3:c.388C>T