Canonical Allele Identifier: PA645494655
Gene: NDUFS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 286051
ClinVar RCV Id: RCV000311823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004541.1:p.Val142Met
CA10605344
NM_004550.5:c.424G>A