Canonical Allele Identifier: PA2826239781
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1941206
ClinVar RCV Id: RCV002643024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186220.1:p.Ser202Pro
CA360866260
NM_001199291.3:c.604T>C