Canonical Allele Identifier: PA2828119065
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2097662
ClinVar RCV Id: RCV003018918
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Gly418Arg
CA346501849
NM_001363823.2:c.1252G>A
CA346501851
NM_001363823.2:c.1252G>C