Canonical Allele Identifier: PA658810274
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 536442
ClinVar RCV Id: RCV000644893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Arg450Gly
CA346502217
NM_014946.4:c.1348A>G