Canonical Allele Identifier: PA916018611
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 591993
ClinVar RCV Id: RCV000723176
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278957.1:p.Asn46Ile
CA360866320
NM_001292028.2:c.137A>T