Canonical Allele Identifier: PA2830441499
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 212291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Ile573Val
CA208917
NM_199436.2:c.1717A>G