Canonical Allele Identifier: PA2828733301
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 536436
ClinVar RCV Id: RCV000644886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Phe336Ser
CA346501201
NM_001377959.1:c.1007T>C