Canonical Allele Identifier: PA2828118735
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1061785
ClinVar RCV Id: RCV001371432
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Leu66Phe
CA346601656
NM_001363823.2:c.198G>C
CA346601657
NM_001363823.2:c.198G>T