Canonical Allele Identifier: PA2830441231
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 960966
ClinVar RCV Id: RCV001234587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Ala463Ser
CA346502530
NM_199436.2:c.1387G>T