Canonical Allele Identifier: PA2573290368
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1393372
ClinVar RCV Id: RCV001898272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Leu262Phe
CA7807950
NM_032520.5:c.786G>C
CA394188754
NM_032520.5:c.786G>T