Allele Registry

Canonical Allele Identifier: PA645496676

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000218324

RCV000301707

RCV000361158

RCV000966445

RCV001079319

RCV002494555

ClinVar Variation:

226669

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186220.1:p.Thr712Ile	CA3382504 NM_001199291.3:c.2135C>T