Canonical Allele Identifier: PA2828733422
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 280383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Asp412Gly
CA10602853
NM_001377959.1:c.1235A>G