Canonical Allele Identifier: PA2741870963
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2575875
ClinVar RCV Id: RCV003321441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361432.1:p.Val73Leu
CA360866876
NM_001374503.1:c.217G>C
CA360866877
NM_001374503.1:c.217G>T