Canonical Allele Identifier: PA2828733350
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 448442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Ser367Leu
CA346501410
NM_001377959.1:c.1100C>T