Canonical Allele Identifier: PA2828125366
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 219575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Arg470Trp
CA348315
NM_001363875.2:c.1408C>T