Canonical Allele Identifier: PA2825378177
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 1735970
ClinVar RCV Id: RCV002357443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030590.1:p.Asn77Ser
CA343456722
NM_001035513.2:c.230A>G