Canonical Allele Identifier: PA645472141
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 409029
ClinVar RCV Id: RCV000464226
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Pro38Arg
CA16610961
NM_014946.4:c.113C>G