Canonical Allele Identifier: PA2826239773
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 872349
ClinVar RCV Id: RCV001092768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186220.1:p.Gln186Glu
CA3381866
NM_001199291.3:c.556C>G