Canonical Allele Identifier: PA2580483049
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1910434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Thr271Arg
CA7807960
NM_032520.5:c.812C>G