Canonical Allele Identifier: PA2826466048
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91047
ClinVar RCV Id: RCV000411744 RCV000691322 RCV001016615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile864Met
CA020945
NM_001258281.1:c.2592A>G