Canonical Allele Identifier: PA2828733358
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Ile374Val
CA253568
NM_001377959.1:c.1120A>G