Canonical Allele Identifier: PA2828125198
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 448442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Ser366Leu
CA346501410
NM_001363875.2:c.1097C>T