Canonical Allele Identifier: PA2828733485
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 521854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Asn455Asp
CA346502475
NM_001377959.1:c.1363A>G