Canonical Allele Identifier: PA2826465509
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479831
ClinVar RCV Id: RCV000575701 RCV003767107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln727Arg
CA346730091
NM_001258281.1:c.2180A>G