Canonical Allele Identifier: PA2579922838
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2005063
ClinVar RCV Id: RCV002820742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His839Asn
CA346730731
NM_000251.3:c.2515C>A