Canonical Allele Identifier: PA2826240048
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1392532
ClinVar RCV Id: RCV001882203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186221.1:p.Asp26Val
CA125857517
NM_001199292.2:c.77A>T