Canonical Allele Identifier: PA237498
Gene: PSEN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 191768
ClinVar RCV Id: RCV000172096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000438.2:p.Ser9Gly
CA237497
NM_000447.3:c.25A>G