Canonical Allele Identifier: PA2829789348
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1298799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Phe124Leu
CA346602417
NM_014946.4:c.370T>C
CA346602421
NM_014946.4:c.372C>A
CA346602422
NM_014946.4:c.372C>G