Canonical Allele Identifier: PA2828120999
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 427079
ClinVar RCV Id: RCV000490105 RCV001643206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350779.1:p.Asp411Asn
CA397420893
NM_001363850.1:c.1231G>A