Canonical Allele Identifier: PA645502988
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 407054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.Thr33Met
CA048701
NM_003001.5:c.98C>T