Canonical Allele Identifier: PA2573290312
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1486491
ClinVar RCV Id: RCV002003629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Ser155Asn
CA276657473
NM_032520.5:c.464G>A