Canonical Allele Identifier: PA2828119160
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 521854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Asn486Asp
CA346502475
NM_001363823.2:c.1456A>G