Canonical Allele Identifier: PA2828733391
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1348218
ClinVar RCV Id: RCV002050789
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Glu388Asp
CA346501868
NM_001377959.1:c.1164G>C
CA346501869
NM_001377959.1:c.1164G>T