Canonical Allele Identifier: PA2825660707
Gene: SPG21 HGNC NCBI

Linked Data

ClinVar Variation Id: 2245977
ClinVar RCV Id: RCV004100435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121361.1:p.Arg247Lys
CA392864779
NM_001127889.5:c.740G>A