Canonical Allele Identifier: PA2828125402
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 217003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Asp509Gly
CA277520
NM_001363875.2:c.1526A>G