Canonical Allele Identifier: PA2580383040
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 2097662
ClinVar RCV Id: RCV003018918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055761.2:p.Gly419Arg
CA346501849
NM_014946.4:c.1255G>A
CA346501851
NM_014946.4:c.1255G>C