Canonical Allele Identifier: PA2499293554
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1046783
ClinVar RCV Id: RCV001351386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Thr165Ser
CA7807734
NM_032520.5:c.494C>G
CA394187906
NM_032520.5:c.493A>T