Canonical Allele Identifier: PA2826558857
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_001263435.1:p.Ala90Glu
CA070965
NM_001276506.2:c.269C>A