Canonical Allele Identifier: PA2826239800
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2044553
ClinVar RCV Id: RCV002903774 RCV003317625 RCV003324053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186220.1:p.Arg224Trp
CA3381885
NM_001199291.3:c.670C>T