Canonical Allele Identifier: PA2828733409
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 617749
ClinVar RCV Id: RCV000754869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Ser404Phe
CA346502113
NM_001377959.1:c.1211C>T