Canonical Allele Identifier: PA645397780
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 412358
ClinVar RCV Id: RCV000467274 RCV000853253 RCV000662662 RCV002341056 RCV003476125
ClinVar Variation Id: 1424413
ClinVar RCV Id: RCV001921634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.Phe160Leu
CA3172860
NM_004168.4:c.478T>C
CA16611826
NM_004168.4:c.480T>G
CA359009926
NM_004168.4:c.480T>A