Canonical Allele Identifier: PA106103
Gene: NDUFS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7511
ClinVar RCV Id: RCV000007941 RCV000442702 RCV000762861
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Amino-acid Alleles

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