Canonical Allele Identifier: PA2828118689
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 989164
ClinVar RCV Id: RCV001391567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Gly37Trp
CA346601373
NM_001363823.2:c.109G>T