Canonical Allele Identifier: PA1139724320
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 960966
ClinVar RCV Id: RCV001234587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Ala495Ser
CA346502530
NM_014946.4:c.1483G>T