Canonical Allele Identifier: PA2826819589
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 350468
ClinVar RCV Id: RCV000270907 RCV000326000 RCV001298354 RCV002244837 RCV002523497 RCV003155169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278957.1:p.Arg403His
CA3382344
NM_001292028.2:c.1208G>A