Canonical Allele Identifier: PA2828119257
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 240952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Gly558Arg
CA10581970
NM_001363823.2:c.1672G>C