Canonical Allele Identifier: PA2742033167
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2818589
ClinVar RCV Id: RCV003634758

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Leu50Pro
CA346601474
NM_199436.2:c.149T>C