Canonical Allele Identifier: PA1139748499
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 840086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Val158Ile
CA7807717
NM_032520.5:c.472G>A