Canonical Allele Identifier: PA2826558425
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 3075083
ClinVar RCV Id: RCV004015609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Pro48Thr
CA382617329
NM_001276504.2:c.142C>A