Canonical Allele Identifier: PA658807139
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 533787
ClinVar RCV Id: RCV002233495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002993.1:p.Ala29Val
CA382616965
NM_003002.4:c.86C>T