Canonical Allele Identifier: PA2826558447
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 420665
ClinVar RCV Id: RCV000479419 RCV000569878 RCV002525847
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Asp53Val
CA16619272
NM_001276504.2:c.158A>T