Canonical Allele Identifier: PA658814602
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 534859
ClinVar RCV Id: RCV000642556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079413.3:p.Asp146Ala
CA7535845
NM_025137.4:c.437A>C