Canonical Allele Identifier: PA2826558789
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2573946
ClinVar RCV Id: RCV003318282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Trp66Arg
CA382617202
NM_001276506.2:c.196T>A
CA382617203
NM_001276506.2:c.196T>C