Canonical Allele Identifier: PA645435032
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 317892
ClinVar RCV Id: RCV000398883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Gly261Ser
CA7807948
NM_032520.5:c.781G>A