Canonical Allele Identifier: PA1139748435
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 967579
ClinVar RCV Id: RCV001242535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Tyr101Cys
CA7807593
NM_032520.5:c.302A>G