Canonical Allele Identifier: PA2499241931
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1034763
ClinVar RCV Id: RCV001337531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186220.1:p.Arg89Ser
CA360864466
NM_001199291.3:c.267G>C
CA360864467
NM_001199291.3:c.267G>T