Canonical Allele Identifier: PA2573290351
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1432652
ClinVar RCV Id: RCV001982068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Phe239Leu
CA394188590
NM_032520.5:c.715T>C
CA394188595
NM_032520.5:c.717T>A
CA394188596
NM_032520.5:c.717T>G