Canonical Allele Identifier: PA2825164747
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1941206
ClinVar RCV Id: RCV002643024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Ser177Pro
CA360866260
NM_000414.4:c.529T>C