Canonical Allele Identifier: PA2826463472
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455622
ClinVar RCV Id: RCV000527981 RCV000573534 RCV001800735 RCV003470714 RCV004003755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu236Met
CA346732951
NM_001258281.1:c.706T>A