Canonical Allele Identifier: PA2826819560
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 137617
ClinVar RCV Id: RCV000125466 RCV000672665 RCV003144135 RCV000825530 RCV001849905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278957.1:p.Ile376Thr
CA163183
NM_001292028.2:c.1127T>C