Canonical Allele Identifier: PA2828125263
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Asp408Gly
CA253555
NM_001363875.2:c.1223A>G