ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645494653
Gene: NDUFS2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
293273
ClinVar RCV Id:
RCV000386683
RCV001859752
RCV003343755
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_004541.1:p.Ile113Val
CA1208536
NM_004550.5:c.337A>G