Canonical Allele Identifier: PA2741948921
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2816402
ClinVar RCV Id: RCV003634715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Asn487Lys
CA346502479
NM_014946.4:c.1461T>A
CA346502480
NM_014946.4:c.1461T>G