Canonical Allele Identifier: PA2828118997
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 566837
ClinVar RCV Id: RCV000686755
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Leu379Pro
CA346501275
NM_001363823.2:c.1136T>C