Canonical Allele Identifier: PA2829411899
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_002992.1:p.Trp61Cys
CA343365628
NM_003001.5:c.183G>C
CA343365633
NM_003001.5:c.183G>T