Canonical Allele Identifier: PA2826838559
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 486381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001281261.1:p.Arg297Trp
CA3173067
NM_001294332.2:c.889C>T