Canonical Allele Identifier: PA2828732995
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1430837
ClinVar RCV Id: RCV001931590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Arg7Leu
CA1600455
NM_001377959.1:c.20G>T