Canonical Allele Identifier: PA1139748578
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 966073
ClinVar RCV Id: RCV001240661 RCV001828957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Ile268Leu
CA7807959
NM_032520.5:c.802A>C