Canonical Allele Identifier: PA113453
Gene: NDUFS7 HGNC NCBI

Linked Data

ClinVar Variation Id: 7681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077718.3:p.Val122Met
CA118993
NM_024407.5:c.364G>A