Canonical Allele Identifier: PA2499293551
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1042823
ClinVar RCV Id: RCV001346838 RCV001831129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Arg147Trp
CA7807703
NM_032520.5:c.439C>T