Canonical Allele Identifier: PA2828733401
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2811936
ClinVar RCV Id: RCV003634654

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Phe395Leu
CA346502053
NM_001377959.1:c.1183T>C
CA346502058
NM_001377959.1:c.1185T>A
CA346502059
NM_001377959.1:c.1185T>G