Canonical Allele Identifier: PA2580569943
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1901782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Pro25Ala
CA346601307
NM_199436.2:c.73C>G