Canonical Allele Identifier: PA2825377992
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 407053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030590.1:p.Ala3Ser
CA048618
NM_001035513.2:c.7G>T