Canonical Allele Identifier: PA645472352
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 280383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Asp444Gly
CA10602853
NM_014946.4:c.1331A>G