Canonical Allele Identifier: PA2826377891
Gene: PGAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50506
ClinVar RCV Id: RCV000043539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243166.1:p.Thr160Ile
CA143757
NM_001256237.1:c.479C>T