Canonical Allele Identifier: PA2573290371
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1363540
ClinVar RCV Id: RCV001902319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Leu263Phe
CA276659295
NM_032520.5:c.787C>T