Canonical Allele Identifier: PA2828119045
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 963588
ClinVar RCV Id: RCV001237635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Ser409Arg
CA346501478
NM_001363823.2:c.1225A>C
CA346501484
NM_001363823.2:c.1227T>A
CA346501485
NM_001363823.2:c.1227T>G