Canonical Allele Identifier: PA2573315386
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 1428531
ClinVar RCV Id: RCV001936355
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955468.1:p.Ser17Arg
CA1600466
NM_199436.2:c.49A>C
CA346601266
NM_199436.2:c.51C>A
CA346601267
NM_199436.2:c.51C>G