Canonical Allele Identifier: PA658674621
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 468565
ClinVar RCV Id: RCV000526604
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Gly471Asp
CA346502364
NM_014946.4:c.1412G>A
CA2586964768
NM_014946.4:c.1412_1413delinsAC