Canonical Allele Identifier: PA2826558814
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412516
ClinVar RCV Id: RCV002230841 RCV003476145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Leu75Ser
CA16613467
NM_001276506.2:c.224T>C