Canonical Allele Identifier: PA1139748563
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 960040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Arg258Lys
CA7807945
NM_032520.5:c.773G>A