Canonical Allele Identifier: PA2826558103
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 840833
ClinVar RCV Id: RCV002239340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Ala13Gly
CA382616724
NM_001276503.2:c.38C>G