Canonical Allele Identifier: PA658810260
Gene: SPAST HGNC NCBI
ClinVar RCV:
RCV000644886
ClinVar Variation:
536436
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Phe368Ser
CA346501201
NM_014946.4:c.1103T>C