Canonical Allele Identifier: PA645482748
Gene: SPG21 HGNC NCBI

Linked Data

ClinVar Variation Id: 316720
ClinVar RCV Id: RCV000705591 RCV000713450 RCV001642988 RCV001848660
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057714.1:p.Ala180Thr
CA7612942
NM_016630.7:c.538G>A