Canonical Allele Identifier: PA645502998
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 239449
ClinVar RCV Id: RCV000227923 RCV002392696 RCV001770197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.His55Arg
CA10581737
NM_003001.5:c.164A>G