Canonical Allele Identifier: PA2829789255
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 989164
ClinVar RCV Id: RCV001391567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Gly37Trp
CA346601373
NM_014946.4:c.109G>T