Canonical Allele Identifier: PA2499293549
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1063370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.His109Gln
CA7807640
NM_032520.5:c.327C>G
CA394187194
NM_032520.5:c.327C>A