This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA2741956073
Gene: NDUFA13 HGNC NCBI
ClinVar RCV:
RCV003376425
ClinVar Variation:
2614074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057049.5:p.Pro11Thr
CA9327609
NM_015965.7:c.31C>A