Canonical Allele Identifier: PA658808197
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 533739
ClinVar RCV Id: RCV000640984 RCV004526729
ClinVar Variation Id: 586670
ClinVar RCV Id: RCV000713482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003110.1:p.Gly672Arg
CA8244506
NM_003119.4:c.2014G>A
CA397434094
NM_003119.4:c.2014G>C