Allele Registry

Canonical Allele Identifier: PA2828526369

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV001937673

ClinVar Variation:

1406932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361431.1:p.Arg111Gly	CA360867149 NM_001374502.1:c.331C>G