Canonical Allele Identifier: PA2826558121
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1413592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263432.1:p.Leu19Pro
CA071527
NM_001276503.2:c.56T>C