Canonical Allele Identifier: PA2828733004
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1405016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Ser13Thr
CA1600460
NM_001377959.1:c.37T>A