Canonical Allele Identifier: PA2573290382
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1469555
ClinVar RCV Id: RCV001961633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Thr274Pro
CA394188819
NM_032520.5:c.820A>C