Canonical Allele Identifier: PA2826558546
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1037130
ClinVar RCV Id: RCV002242215 RCV002329313 RCV003473869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Tyr105His
CA071384
NM_001276504.2:c.313T>C