Canonical Allele Identifier: PA2828733325
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1675775
ClinVar RCV Id: RCV002214144

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Pro351Gln
CA346501295
NM_001377959.1:c.1052C>A