Canonical Allele Identifier: PA2580483048
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1971485
ClinVar RCV Id: RCV002740774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Gly267Cys
CA7807957
NM_032520.5:c.799G>T