Canonical Allele Identifier: PA2826463014
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91139
ClinVar RCV Id: RCV000076643 RCV000160632 RCV000497286 RCV000684796 RCV001353866 RCV003334382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu125del
CA021449
NM_001258281.1:c.373_375del