Canonical Allele Identifier: PA2825377804
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 407061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030589.1:p.Val48Phe
CA047220
NM_001035512.2:c.142G>T