Canonical Allele Identifier: PA2828733039
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 3010987
ClinVar RCV Id: RCV003869650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Pro41Thr
CA1600492
NM_001377959.1:c.121C>A
CA2740092819
NM_001377959.1:c.120_121delinsAA