Canonical Allele Identifier: PA2828525135
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2575875
ClinVar RCV Id: RCV003321441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361428.1:p.Val101Leu
CA360866876
NM_001374499.1:c.301G>C
CA360866877
NM_001374499.1:c.301G>T