Canonical Allele Identifier: PA2825892593
Gene: PGAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50503
ClinVar RCV Id: RCV000043536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138910.1:p.Arg230Pro
CA5829883
NM_001145438.2:c.689G>C