Canonical Allele Identifier: PA2825381590
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_001032900.1:p.Ala95Val
CA10421018
NM_001037811.2:c.284C>T