Canonical Allele Identifier: PA2826558179
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 641815
ClinVar RCV Id: RCV002535923 RCV004027515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Ile40Thr
CA382617025
NM_001276503.2:c.119T>C