Canonical Allele Identifier: PA2828119092
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Asp440Gly
CA253555
NM_001363823.2:c.1319A>G