Canonical Allele Identifier: PA2828119261
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 217004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Arg561Gln
CA278930
NM_001363823.2:c.1682G>A