Canonical Allele Identifier: PA196697
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 187084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.His127Arg
CA011435
NM_003001.5:c.380A>G