Canonical Allele Identifier: PA2826818778
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_001278956.1:p.Gln137Pro
CA3381867
NM_001292027.2:c.410A>C