Canonical Allele Identifier: PA095375
Gene: HSD17B10 HGNC NCBI

Linked Data

ClinVar Variation Id: 11443
ClinVar RCV Id: RCV000012196 RCV002307362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004484.1:p.Leu122Val
CA121451
NM_004493.3:c.364C>G