Canonical Allele Identifier: PA2828125330
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 536441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Thr453Ala
CA346502469
NM_001363875.2:c.1357A>G