Allele Registry

Canonical Allele Identifier: PA2826819511

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000410433

RCV001387756

ClinVar Variation:

371413

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278957.1:p.Asn317Asp	CA3382214 NM_001292028.2:c.949A>G