Canonical Allele Identifier: PA130382
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 39585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.Thr508Ile
CA130381
NM_004168.4:c.1523C>T