Allele Registry

Canonical Allele Identifier: PA2826819030

Gene: HSD17B4 HGNC NCBI

ClinVar RCV:

RCV000410433

RCV001387756

ClinVar Variation:

371413

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278956.1:p.Asn433Asp	CA3382214 NM_001292027.2:c.1297A>G