Canonical Allele Identifier: PA2580385363
Gene: NDUFA13 HGNC NCBI
ClinVar RCV:
RCV002691596
ClinVar Variation:
2217053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057049.5:p.Val6Ala
CA306360469
NM_015965.7:c.17T>C