Allele Registry

Canonical Allele Identifier: PA2826819327

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV001937673

ClinVar Variation:

1406932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278957.1:p.Arg108Gly	CA360867149 NM_001292028.2:c.322C>G