Canonical Allele Identifier: PA916018607
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 191198
ClinVar RCV Id: RCV000171384 RCV003987412
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278956.1:p.His99Asp
CA236235
NM_001292027.2:c.295C>G