Canonical Allele Identifier: PA2826240130
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1713648
ClinVar RCV Id: RCV002304279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186221.1:p.Tyr146Cys
CA360866180
NM_001199292.2:c.437A>G