Canonical Allele Identifier: PA916055809
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 644235
ClinVar RCV Id: RCV000798114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Ala1909Thr
CA7534361
NM_025137.4:c.5725G>A