Canonical Allele Identifier: PA2826240598
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 287598
ClinVar RCV Id: RCV000401079 RCV002227469 RCV002518987 RCV004543107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186221.1:p.Leu708Val
CA3382536
NM_001199292.2:c.2122C>G