Canonical Allele Identifier: PA645494706
Gene: NDUFA13 HGNC NCBI

Linked Data

ClinVar Variation Id: 132643
ClinVar RCV Id: RCV000239442 RCV000735414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057049.5:p.Arg57His
CA9327697
NM_015965.7:c.170G>A