Canonical Allele Identifier: PA2829789261
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 3010987
ClinVar RCV Id: RCV003869650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Pro41Thr
CA1600492
NM_014946.4:c.121C>A
CA2740092819
NM_014946.4:c.120_121delinsAA