Canonical Allele Identifier: PA916069480
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 718947
ClinVar RCV Id: RCV000891982 RCV001276185 RCV003940700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Arg272Gly
CA7807962
NM_032520.5:c.814A>G