Canonical Allele Identifier: PA2827370497
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_001333326.1:p.Thr154Ile
CA143757
NM_001346397.2:c.461C>T