Canonical Allele Identifier: PA2573290285
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1359569
ClinVar RCV Id: RCV001872288
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Trp111Arg
CA7807642
NM_032520.5:c.331T>C
CA394187208
NM_032520.5:c.331T>A