Canonical Allele Identifier: PA2826819109
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 137619
ClinVar RCV Id: RCV000125468 RCV000730879 RCV001849906 RCV003467098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278956.1:p.Arg519Pro
CA163187
NM_001292027.2:c.1556G>C