Canonical Allele Identifier: PA2825377914
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 142904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030589.1:p.Pro112Thr
CA016343
NM_001035512.2:c.334C>A