Canonical Allele Identifier: PA2829789247
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 657662
ClinVar RCV Id: RCV000814318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Ala30Val
CA1600478
NM_014946.4:c.89C>T