Canonical Allele Identifier: PA323967
Gene: NDUFS4 HGNC NCBI

Linked Data

ClinVar Variation Id: 214812
ClinVar RCV Id: RCV000199422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002486.1:p.Thr130Ser
CA323966
NM_002495.4:c.389C>G
CA359719190
NM_002495.4:c.388A>T