Canonical Allele Identifier: PA096585
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 963588
ClinVar RCV Id: RCV001237635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Ser410Arg
CA346501478
NM_014946.4:c.1228A>C
CA346501484
NM_014946.4:c.1230T>A
CA346501485
NM_014946.4:c.1230T>G