Canonical Allele Identifier: PA2826838900
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 1055638
ClinVar RCV Id: RCV001364342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001281261.1:p.Asp411Gly
CA359014032
NM_001294332.2:c.1232A>G