Canonical Allele Identifier: PA2825377573
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 438444
ClinVar RCV Id: RCV000505336

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030588.1:p.Gly73Asp
CA343365949
NM_001035511.2:c.218G>A