Canonical Allele Identifier: PA331684
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91208
ClinVar RCV Id: RCV000076712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln264His
CA022289
NM_000251.3:c.792G>C
CA346732533
NM_000251.3:c.792G>T