Allele Registry

Canonical Allele Identifier: PA106103

Gene: NDUFS8 HGNC NCBI

ClinVar RCV:

RCV000007941

RCV000442702

RCV000762861

ClinVar Variation:

7511

HGVS (amino-acid)	Matching Registered Transcripts
NP_002487.1:p.Pro79Leu	CA118853 NM_002496.4:c.236C>T