Canonical Allele Identifier: PA2580483047
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 2164295
ClinVar RCV Id: RCV003087959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Gly261Ala
CA394188748
NM_032520.5:c.782G>C