Canonical Allele Identifier: PA105389
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7655
ClinVar RCV Id: RCV000008094 RCV000415821 RCV000688945 RCV000779455 RCV001197145 RCV002512888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Gly16Ser
CA118960
NM_000414.4:c.46G>A