Canonical Allele Identifier: PA2828125315
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 468565
ClinVar RCV Id: RCV000526604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Gly438Asp
CA346502364
NM_001363875.2:c.1313G>A
CA2586964768
NM_001363875.2:c.1313_1314delinsAC