Canonical Allele Identifier: PA2828120823
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 215185
ClinVar RCV Id: RCV000197933 RCV001853199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350779.1:p.Asp135Asn
CA322399
NM_001363850.1:c.403G>A