Canonical Allele Identifier: PA1139748576
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 971493
ClinVar RCV Id: RCV001247285 RCV001835294
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.His266Gln
CA7807954
NM_032520.5:c.798C>A
CA394188777
NM_032520.5:c.798C>G