Canonical Allele Identifier: PA325092
Gene: NDUFS4 HGNC NCBI

Linked Data

ClinVar Variation Id: 214810
ClinVar RCV Id: RCV000335188 RCV000960853 RCV001154576 RCV001154575
ClinVar Variation Id: 419348
ClinVar RCV Id: RCV000478751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002486.1:p.Val4Leu
CA325091
NM_002495.4:c.10G>C
CA16618208
NM_002495.4:c.10_12delinsCTC
CA359718936
NM_002495.4:c.10G>T