Canonical Allele Identifier: PA2826558742
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 431847
ClinVar RCV Id: RCV000497964 RCV000569506 RCV000505346 RCV002230973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.His50Asp
CA382617089
NM_001276506.2:c.148C>G