Canonical Allele Identifier: PA2580467732
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2037072
ClinVar RCV Id: RCV002885479 RCV004065955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Leu1776Phe
CA392222789
NM_025137.4:c.5326C>T