Canonical Allele Identifier: PA2828118790
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 989166
ClinVar RCV Id: RCV001391569
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Val118Leu
CA346602372
NM_001363823.2:c.352G>C