Canonical Allele Identifier: PA2826240151
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1522331
ClinVar RCV Id: RCV002034370 RCV002222752
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186221.1:p.Ala178Val
CA3381883
NM_001199292.2:c.533C>T