Canonical Allele Identifier: PA916069448
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 739773
ClinVar RCV Id: RCV000915776 RCV001832067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Ala160Val
CA7807721
NM_032520.5:c.479C>T