Canonical Allele Identifier: PA2826240128
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 907603
ClinVar RCV Id: RCV001157566 RCV001157565 RCV001772352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186221.1:p.Gln143Pro
CA3381867
NM_001199292.2:c.428A>C