Canonical Allele Identifier: PA1139743438
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 872349
ClinVar RCV Id: RCV001092768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361428.1:p.Gln52Glu
CA3381866
NM_001374499.1:c.154C>G