Canonical Allele Identifier: PA2828125271
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 280383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Asp411Gly
CA10602853
NM_001363875.2:c.1232A>G