Canonical Allele Identifier: PA2828733056
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 835946
ClinVar RCV Id: RCV001036951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Tyr51Cys
CA346601485
NM_001377959.1:c.152A>G