Canonical Allele Identifier: PA2826558616
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 1436049
ClinVar RCV Id: RCV001974679
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Leu7Pro
CA382616669
NM_001276506.2:c.20T>C