Canonical Allele Identifier: PA203226
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 198079
ClinVar RCV Id: RCV000179310 RCV000391832 RCV000362861 RCV000676075 RCV001517001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Arg106His
CA203225
NM_000414.4:c.317G>A