Canonical Allele Identifier: PA2828733387
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_001364888.1:p.Gly387Arg
CA346501849
NM_001377959.1:c.1159G>A
CA346501851
NM_001377959.1:c.1159G>C