Canonical Allele Identifier: PA1139748503
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 887093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Ala160Glu
CA7807722
NM_032520.5:c.479C>A