Canonical Allele Identifier: PA2825377378
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 465977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030588.1:p.Ala2Thr
CA343354908
NM_001035511.2:c.4G>A