Canonical Allele Identifier: PA916069447
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 712909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.His150Gln
CA7807707
NM_032520.5:c.450T>G
CA394187747
NM_032520.5:c.450T>A