Canonical Allele Identifier: PA2828733339
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 208644
ClinVar RCV Id: RCV000190649 RCV000206286 RCV000478313
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Met358Val
CA204591
NM_001377959.1:c.1072A>G