Canonical Allele Identifier: PA241506
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 195194
ClinVar RCV Id: RCV000175748 RCV002056943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003110.1:p.Leu78Phe
CA241505
NM_003119.4:c.234G>T
CA397416830
NM_003119.4:c.234G>C