Allele Registry

Canonical Allele Identifier: PA2828525559

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV002580362

ClinVar Variation:

1902544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361429.1:p.Arg101Leu	CA360867151 NM_001374500.1:c.302G>T