Canonical Allele Identifier: PA2499293548
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1005964
ClinVar RCV Id: RCV001302926 RCV001835459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.His92Gln
CA7807578
NM_032520.5:c.276C>G
CA394186926
NM_032520.5:c.276C>A