Canonical Allele Identifier: PA2826818799
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1522331
ClinVar RCV Id: RCV002034370 RCV002222752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278956.1:p.Ala172Val
CA3381883
NM_001292027.2:c.515C>T