Canonical Allele Identifier: PA2499293552
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1027074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Ala160Thr
CA7807720
NM_032520.5:c.478G>A