Canonical Allele Identifier: PA645502979
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 239451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.Val9Ile
CA047404
NM_003001.5:c.25G>A