Canonical Allele Identifier: PA645503015
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 239453
ClinVar RCV Id: RCV000231142 RCV000482240 RCV002256145 RCV003475064 RCV003507270 RCV003998863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002992.1:p.Tyr99His
CA047136
NM_003001.5:c.295T>C