Canonical Allele Identifier: PA645503025
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 407059
ClinVar RCV Id: RCV000477028 RCV001770321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.Trp129Cys
CA16609905
NM_003001.5:c.387G>C
CA343456714
NM_003001.5:c.387G>T