Allele Registry

Canonical Allele Identifier: PA2826819703

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000218324

RCV000301707

RCV000361158

RCV000966445

RCV001079319

RCV002494555

ClinVar Variation:

226669

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278957.1:p.Thr547Ile	CA3382504 NM_001292028.2:c.1640C>T