Canonical Allele Identifier: PA2826839235
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 160358
ClinVar Variation Id: 568815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001281261.1:p.Arg537Trp
CA188615
NM_001294332.2:c.1609C>T
CA891842547
NM_001294332.2:c.1608_1609delinsGT