Canonical Allele Identifier: PA2826582288
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 801278
ClinVar Variation Id: 2068240
ClinVar RCV Id: RCV002971009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265101.1:p.Trp27Cys
CA343365628
NM_001278172.2:c.81G>C
CA343365633
NM_001278172.2:c.81G>T