Canonical Allele Identifier: PA916069475
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 645813
ClinVar RCV Id: RCV000799973 RCV001825578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Pro269His
CA394188791
NM_032520.5:c.806C>A