Canonical Allele Identifier: PA2580569959
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2154832
ClinVar RCV Id: RCV003069485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Arg48Trp
CA346601449
NM_199436.2:c.142C>T