Canonical Allele Identifier: PA2826463267
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237405
ClinVar RCV Id: RCV000230625 RCV000564902 RCV001557291 RCV003463649 RCV003998764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln186Arg
CA040278
NM_001258281.1:c.557A>G