Allele Registry

Canonical Allele Identifier: PA2826819031

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000008095

RCV000385297

RCV000477799

RCV000684773

RCV001002204

ClinVar Variation:

7656

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278956.1:p.Asn433Tyr	CA118961 NM_001292027.2:c.1297A>T