Canonical Allele Identifier: PA2499235938
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 1021759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030589.1:p.Leu86Arg
CA343456617
NM_001035512.2:c.257T>G