Canonical Allele Identifier: PA2829789252
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1038883
ClinVar RCV Id: RCV001342255

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Pro34Leu
CA1600484
NM_014946.4:c.101C>T