Canonical Allele Identifier: PA2579922975
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2831992
ClinVar RCV Id: RCV003758288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys847Asn
CA346730837
NM_000251.3:c.2541A>C
CA346730839
NM_000251.3:c.2541A>T