Canonical Allele Identifier: PA2828733465
Gene: SPAST HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Asp438Val
CA253564
NM_001377959.1:c.1313A>T