Canonical Allele Identifier: PA2826582211
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 161387
ClinVar RCV Id: RCV000148872 RCV000471140 RCV000563869 RCV002464125 RCV002465536 RCV003998177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265101.1:p.Ala3Val
CA011497
NM_001278172.2:c.8C>T