Canonical Allele Identifier: PA2828119067
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1348218
ClinVar RCV Id: RCV002050789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Glu419Asp
CA346501868
NM_001363823.2:c.1257G>C
CA346501869
NM_001363823.2:c.1257G>T