Canonical Allele Identifier: PA2826582326
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 189841

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265101.1:p.Gly41Asp
CA016245
NM_001278172.2:c.122G>A