Canonical Allele Identifier: PA2825377770
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 1940562
ClinVar RCV Id: RCV002658470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030589.1:p.Met33Ile
CA343365794
NM_001035512.2:c.99G>A
CA343365796
NM_001035512.2:c.99G>C
CA343365799
NM_001035512.2:c.99G>T