Canonical Allele Identifier: PA658802654
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 504931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Val37Ile
CA3381664
NM_000414.4:c.109G>A