Canonical Allele Identifier: PA2825946816
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 566795
ClinVar RCV Id: RCV000686707 RCV000761910 RCV001644765 RCV002442422 RCV002468001 RCV002468002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153699.1:p.Pro102Ser
CA7535873
NM_001160227.2:c.304C>T