Canonical Allele Identifier: PA2573290360
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 1463840
ClinVar RCV Id: RCV001975302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Ser253Pro
CA7807939
NM_032520.5:c.757T>C