Canonical Allele Identifier: PA2829789265
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 897738
ClinVar RCV Id: RCV001141200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Glu43Asp
CA1600498
NM_014946.4:c.129G>C
CA346601405
NM_014946.4:c.129G>T