Canonical Allele Identifier: PA2826558859
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 412511
ClinVar RCV Id: RCV000562410 RCV001821298 RCV001584171 RCV002230663
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Ala90Val
CA070974
NM_001276506.2:c.269C>T