Canonical Allele Identifier: PA2580483029
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 2162479
ClinVar RCV Id: RCV003091298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Ala173Thr
CA7807749
NM_032520.5:c.517G>A