Canonical Allele Identifier: PA2825381584
Gene: HSD17B10 HGNC NCBI

Linked Data

ClinVar Variation Id: 435470
ClinVar RCV Id: RCV000504036 RCV000766098 RCV001857111 RCV004023377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001032900.1:p.Val87Ile
CA10421022
NM_001037811.2:c.259G>A