Canonical Allele Identifier: PA2828733508
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Arg467Cys
CA253551
NM_001377959.1:c.1399C>T