Canonical Allele Identifier: PA2828125408
Gene: SPAST HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Gly513Glu
CA333996
NM_001363875.2:c.1538G>A