Canonical Allele Identifier: PA2580483027
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 2364614
ClinVar RCV Id: RCV002984485 RCV003561145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Pro171Ser
CA394187936
NM_032520.5:c.511C>T