Canonical Allele Identifier: PA2825164679
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1034763
ClinVar RCV Id: RCV001337531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Arg64Ser
CA360864466
NM_000414.4:c.192G>C
CA360864467
NM_000414.4:c.192G>T