Canonical Allele Identifier: PA2828125186
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 208644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Met357Val
CA204591
NM_001363875.2:c.1069A>G