Canonical Allele Identifier: PA2828125216
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 963588
ClinVar RCV Id: RCV001237635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Ser377Arg
CA346501478
NM_001363875.2:c.1129A>C
CA346501484
NM_001363875.2:c.1131T>A
CA346501485
NM_001363875.2:c.1131T>G