Canonical Allele Identifier: PA2825377523
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 239449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030588.1:p.His55Arg
CA10581737
NM_001035511.2:c.164A>G