Canonical Allele Identifier: PA658671905
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455612
ClinVar RCV Id: RCV000554397 RCV003459181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu262Gln
CA346732493
NM_000251.3:c.784G>C