ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828711228
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_001364230.1:p.Ile113Val
CA1208536
NM_001377301.1:c.337A>G