Canonical Allele Identifier: PA2828524682
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3107137
ClinVar RCV Id: RCV004404491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361427.1:p.Arg110Gly
CA3381788
NM_001374498.1:c.328A>G