Canonical Allele Identifier: PA913194115
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 617765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Glu418del
CA913190206
NM_014946.4:c.1253_1255del