Canonical Allele Identifier: PA658831926
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 553608
ClinVar RCV Id: RCV000669091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Arg272del
CA658824130
NM_032520.5:c.814_816del