Canonical Allele Identifier: PA2499267962
Gene: HSD17B10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1021779
ClinVar RCV Id: RCV001321597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004484.1:p.Ala95Val
CA10421018
NM_004493.3:c.284C>T