Canonical Allele Identifier: PA201314
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 194706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000405.1:p.Ala491Thr
CA201313
NM_000414.4:c.1471G>A