Canonical Allele Identifier: PA2826558439
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412512
ClinVar RCV Id: RCV001016345 RCV001252746 RCV002230664 RCV003235231
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263433.1:p.Ala51Glu
CA070965
NM_001276504.2:c.152C>A