Canonical Allele Identifier: PA2825378198
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 142904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030590.1:p.Pro93Thr
CA016343
NM_001035513.2:c.277C>A