Canonical Allele Identifier: PA2825660761
Gene: SPG21 HGNC NCBI

Linked Data

ClinVar Variation Id: 316720
ClinVar RCV Id: RCV000705591 RCV000713450 RCV001642988 RCV001848660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121362.1:p.Ala153Thr
CA7612942
NM_001127890.5:c.457G>A