Canonical Allele Identifier: PA209578
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 212142
ClinVar RCV Id: RCV000195027 RCV000663178
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.Val425Gly
CA209577
NM_004168.4:c.1274T>G