Canonical Allele Identifier: PA2827348395
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 1769994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317687.1:p.Ala442Val
CA359013933
NM_001330758.2:c.1325C>T