Canonical Allele Identifier: PA2826240126
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1335590
ClinVar RCV Id: RCV001816401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186221.1:p.Ser135Leu
CA360866104
NM_001199292.2:c.404C>T