Canonical Allele Identifier: PA2499293559
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1042407
ClinVar RCV Id: RCV001346359 RCV001836342 RCV002547058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Thr211Ser
CA7807857
NM_032520.5:c.631A>T