Canonical Allele Identifier: PA658831916
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 550212
ClinVar RCV Id: RCV000664893 RCV001037602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Lys80_Tyr81del
CA7807562
NM_032520.5:c.238_243del
CA912994972
NM_032520.5:c.240_242del