Canonical Allele Identifier: PA2830440879
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 397539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Leu339Phe
CA16609412
NM_199436.2:c.1015C>T