Canonical Allele Identifier: PA2826239806
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_001186220.1:p.Val235Leu
CA360866876
NM_001199291.3:c.703G>C
CA360866877
NM_001199291.3:c.703G>T