Canonical Allele Identifier: PA2828526713
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_001361432.1:p.Gln24Pro
CA3381867
NM_001374503.1:c.71A>C