Canonical Allele Identifier: PA2829789232
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1428531
ClinVar RCV Id: RCV001936355

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Ser17Arg
CA1600466
NM_014946.4:c.49A>C
CA346601266
NM_014946.4:c.51C>A
CA346601267
NM_014946.4:c.51C>G