Canonical Allele Identifier: PA916006691
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 809726

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.Ser509Trp
CA112829740
NM_004168.4:c.1526C>G