Canonical Allele Identifier: PA2828124942
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 586664
ClinVar RCV Id: RCV000713471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350804.1:p.Phe82Leu
CA346601889
NM_001363875.2:c.244T>C
CA346601903
NM_001363875.2:c.246C>A
CA346601905
NM_001363875.2:c.246C>G