Canonical Allele Identifier: PA236238
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 191199
ClinVar RCV Id: RCV000171385 RCV003987413 RCV003765072 RCV003317125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Asn176Asp
CA236237
NM_000414.4:c.526A>G