Canonical Allele Identifier: PA2826558359
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2948182
ClinVar RCV Id: RCV003807004
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Ala22Pro
CA382617173
NM_001276504.2:c.64G>C