Canonical Allele Identifier: PA2573260529
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1675775
ClinVar RCV Id: RCV002214144

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Pro383Gln
CA346501295
NM_014946.4:c.1148C>A