Canonical Allele Identifier: PA2741948917
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2811936
ClinVar RCV Id: RCV003634654

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Phe427Leu
CA346502053
NM_014946.4:c.1279T>C
CA346502058
NM_014946.4:c.1281T>A
CA346502059
NM_014946.4:c.1281T>G