Canonical Allele Identifier: PA2828099488
Gene: NDUFS7 HGNC NCBI

Linked Data

ClinVar Variation Id: 7681
ClinVar RCV Id: RCV000008120 RCV000197296 RCV003155020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350531.1:p.Val122Met
CA118993
NM_001363602.2:c.364G>A