Canonical Allele Identifier: PA2826465357
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90943
ClinVar RCV Id: RCV000076445 RCV000561670 RCV003452902
ClinVar Variation Id: 439192
ClinVar RCV Id: RCV000508314 RCV000680198 RCV001014940 RCV003593976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly685Arg
CA020361
NM_001258281.1:c.2053G>A
CA346729765
NM_001258281.1:c.2053G>C