Canonical Allele Identifier: PA2828711218
Gene: NDUFS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364230.1:p.Pro71Leu
CA321381
NM_001377301.1:c.212C>T