Canonical Allele Identifier: PA349348
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 219638
ClinVar RCV Id: RCV000205153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003110.1:p.Ile219Thr
CA349347
NM_003119.4:c.656T>C