Canonical Allele Identifier: PA2828524233
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685886
ClinVar RCV Id: RCV002250053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361426.1:p.Leu175Phe
CA360866267
NM_001374497.1:c.523C>T