Canonical Allele Identifier: PA2828124963
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 3168170
ClinVar RCV Id: RCV004460084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Ala104Thr
CA346602231
NM_001363875.2:c.310G>A