Canonical Allele Identifier: PA2828125215
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 418502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Ala376Thr
CA16617528
NM_001363875.2:c.1126G>A