Canonical Allele Identifier: PA2828733361
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 665622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Ser375Asn
CA346501463
NM_001377959.1:c.1124G>A