Canonical Allele Identifier: PA206848
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 212143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.Val531Met
CA206847
NM_004168.4:c.1591G>A