Canonical Allele Identifier: PA2828124962
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2397438
ClinVar RCV Id: RCV002710032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Ala104Pro
CA346602234
NM_001363875.2:c.310G>C