Canonical Allele Identifier: PA2828733073
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1707912
ClinVar RCV Id: RCV002287073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Phe61Leu
CA346601599
NM_001377959.1:c.181T>C
CA346601609
NM_001377959.1:c.183C>A
CA346601611
NM_001377959.1:c.183C>G