Canonical Allele Identifier: PA2828125471
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 212291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Ile572Val
CA208917
NM_001363875.2:c.1714A>G