Canonical Allele Identifier: PA1139748584
Gene: GNPTG HGNC NCBI

Linked Data

ClinVar Variation Id: 963830
ClinVar RCV Id: RCV001237920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115909.1:p.Pro269Ser
CA394188790
NM_032520.5:c.805C>T