Canonical Allele Identifier: PA2828125207
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Ile373Val
CA253568
NM_001363875.2:c.1117A>G