Canonical Allele Identifier: PA645472257
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 432721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Leu371Arg
CA346501219
NM_014946.4:c.1112T>G