Canonical Allele Identifier: PA2828119180
Gene: SPAST HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Arg497Ser
CA346502816
NM_001363823.2:c.1491G>C
CA346502817
NM_001363823.2:c.1491G>T