Allele Registry

Canonical Allele Identifier: PA2828525469

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000218324

RCV000301707

RCV000361158

RCV000966445

RCV001079319

RCV002494555

ClinVar Variation:

226669

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361428.1:p.Thr578Ile	CA3382504 NM_001374499.1:c.1733C>T