Canonical Allele Identifier: PA2825377894
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 1737359
ClinVar RCV Id: RCV002321278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030589.1:p.Leu101Ser
CA343456775
NM_001035512.2:c.302T>C