Canonical Allele Identifier: PA658810291
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 536434
ClinVar RCV Id: RCV000644884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Arg498Ser
CA346502816
NM_014946.4:c.1494G>C
CA346502817
NM_014946.4:c.1494G>T