Canonical Allele Identifier: PA2826558578
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 2032648
ClinVar RCV Id: RCV002881330
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Lys119_Leu120delinsAsnPhe
CA2580083599
NM_001276504.2:c.357_358delinsTT