Canonical Allele Identifier: PA2828733506
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1335894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Arg466Thr
CA346502548
NM_001377959.1:c.1397G>C