Canonical Allele Identifier: PA2826582209
Gene: SDHC HGNC NCBI

Linked Data

ClinVar Variation Id: 465977
ClinVar RCV Id: RCV000542616 RCV003159828 RCV003476281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265101.1:p.Ala2Thr
CA343354908
NM_001278172.2:c.4G>A