Canonical Allele Identifier: PA891853817
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 581048
ClinVar RCV Id: RCV000704760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.Ala454Ser
CA359013999
NM_004168.4:c.1360G>T