Canonical Allele Identifier: PA2573290315
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1418597
ClinVar RCV Id: RCV001952194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Thr165Ile
CA276657637
NM_032520.5:c.494C>T