Canonical Allele Identifier: PA2828733131
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2222971
ClinVar RCV Id: RCV002678195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Val116Gly
CA346602364
NM_001377959.1:c.347T>G