Canonical Allele Identifier: PA2830440938
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Asn354Ser
CA253562
NM_199436.2:c.1061A>G