Allele Registry

Canonical Allele Identifier: PA2826818743

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000008096

ClinVar Variation:

7657

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278956.1:p.Arg82Pro	CA118962 NM_001292027.2:c.245G>C