Canonical Allele Identifier: PA658810285
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 521854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Asn487Asp
CA346502475
NM_014946.4:c.1459A>G