Canonical Allele Identifier: PA2830441006
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 418502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Ala377Thr
CA16617528
NM_199436.2:c.1129G>A