Canonical Allele Identifier: PA274908
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 193253
ClinVar RCV Id: RCV000173302 RCV001852108 RCV003416067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003110.1:p.Met1Val