Canonical Allele Identifier: PA253572
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5676
ClinVar RCV Id: RCV000006030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Ser445Arg
CA253570
NM_014946.4:c.1335C>A
CA346502182
NM_014946.4:c.1333A>C
CA346502188
NM_014946.4:c.1335C>G