Canonical Allele Identifier: PA2573290355
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1399781
ClinVar RCV Id: RCV001917856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Ala248Ser
CA7807932
NM_032520.5:c.742G>T