Canonical Allele Identifier: PA2828125252
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 432722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Arg398Gln
CA346502079
NM_001363875.2:c.1193G>A