Allele Registry

Canonical Allele Identifier: PA916003161

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000410433

RCV001387756

ClinVar Variation:

371413

HGVS (amino-acid)	Matching Registered Transcripts
NP_001186220.1:p.Asn482Asp	CA3382214 NM_001199291.3:c.1444A>G