Canonical Allele Identifier: PA658807112
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 534377
ClinVar RCV Id: RCV000641922 RCV002256432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.Leu120Phe
CA343456612
NM_003001.5:c.358C>T