Canonical Allele Identifier: PA2826558352
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 638845
ClinVar RCV Id: RCV001013090 RCV002536930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Ser20Phe
CA382617164
NM_001276504.2:c.59C>T