Canonical Allele Identifier: PA2830441232
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 409032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Ala463Thr
CA16610831
NM_199436.2:c.1387G>A