Canonical Allele Identifier: PA2828119145
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_001350752.1:p.Gly470Asp
CA346502364
NM_001363823.2:c.1409G>A
CA2586964768
NM_001363823.2:c.1409_1410delinsAC