Canonical Allele Identifier: PA2826240136
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 191199
ClinVar RCV Id: RCV000171385 RCV003987413 RCV003765072 RCV003317125
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186221.1:p.Asn158Asp
CA236237
NM_001199292.2:c.472A>G