Canonical Allele Identifier: PA1139748304
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 990360
ClinVar RCV Id: RCV001278357
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Thr90Ile
CA276656608
NM_032520.5:c.269C>T