Canonical Allele Identifier: PA2828125432
Gene: SPAST HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Arg529Gly
CA253566
NM_001363875.2:c.1585C>G