Canonical Allele Identifier: PA2828733466
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_001364888.1:p.Gly439Asp
CA346502364
NM_001377959.1:c.1316G>A
CA2586964768
NM_001377959.1:c.1316_1317delinsAC