Canonical Allele Identifier: PA2826818788
Gene: HSD17B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685886
ClinVar RCV Id: RCV002250053
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278956.1:p.Leu154Phe
CA360866267
NM_001292027.2:c.460C>T