Canonical Allele Identifier: PA2826377799
Gene: PGAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50503
ClinVar RCV Id: RCV000043536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243164.1:p.Arg195Pro
CA5829883
NM_001256235.1:c.584G>C