Canonical Allele Identifier: PA2580140724
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 1735970
ClinVar RCV Id: RCV002357443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030589.1:p.Asn96Ser
CA343456722
NM_001035512.2:c.287A>G