Canonical Allele Identifier: PA2826558821
Gene: SDHD HGNC NCBI

Linked Data

ClinVar Variation Id: 3073872
ClinVar RCV Id: RCV004012414
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263435.1:p.Leu77Gln
CA382617275
NM_001276506.2:c.230T>A