Canonical Allele Identifier: PA2825378045
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 189841

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030590.1:p.Gly22Asp
CA016245
NM_001035513.2:c.65G>A