Canonical Allele Identifier: PA2826239767
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1364464
ClinVar RCV Id: RCV001937461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186220.1:p.Met173Val
CA125861912
NM_001199291.3:c.517A>G