Canonical Allele Identifier: PA645397995
Gene: SDHA HGNC NCBI

Linked Data

ClinVar Variation Id: 239644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004159.2:p.Arg465Trp
CA3173212
NM_004168.4:c.1393C>T