Canonical Allele Identifier: PA2825378081
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 407056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030590.1:p.Ser35Leu
CA047197
NM_001035513.2:c.104C>T