Canonical Allele Identifier: PA2826466062
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127641
ClinVar RCV Id: RCV000115524 RCV000212622 RCV000986691 RCV001086842 RCV001194031 RCV001357791 RCV003997276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr868Met
CA020959
NM_001258281.1:c.2603C>T