Canonical Allele Identifier: PA916003079
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 350463
ClinVar RCV Id: RCV000319617 RCV000374018 RCV000730900 RCV002520294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186220.1:p.Ala296Thr
CA3381989
NM_001199291.3:c.886G>A