Canonical Allele Identifier: PA2825381567
Gene: HSD17B10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2744815
ClinVar RCV Id: RCV003565805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001032900.1:p.Glu48Ala
CA413154301
NM_001037811.2:c.143A>C