Canonical Allele Identifier: PA658706190
Gene: NDUFS8 HGNC NCBI

Linked Data

ClinVar Variation Id: 488561
ClinVar RCV Id: RCV000578254 RCV001815416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002487.1:p.Met147Ile
CA381569169
NM_002496.4:c.441G>A
CA381569172
NM_002496.4:c.441G>C
CA381569174
NM_002496.4:c.441G>T