Canonical Allele Identifier: PA2826582357
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 142904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265101.1:p.Ser57Tyr
CA016343
NM_001278172.2:c.170C>A