Canonical Allele Identifier: PA2828120946
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 436844
ClinVar RCV Id: RCV000501596 RCV001662499 RCV003235255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350779.1:p.Ala345Pro
CA397419954
NM_001363850.1:c.1033G>C