Canonical Allele Identifier: PA2573290374
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1426530
ClinVar RCV Id: RCV001929461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Gly267Ser
CA7807956
NM_032520.5:c.799G>A