Allele Registry

Canonical Allele Identifier: PA2826818849

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV001937673

ClinVar Variation:

1406932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278956.1:p.Arg224Gly	CA360867149 NM_001292027.2:c.670C>G