Canonical Allele Identifier: PA2826463464
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142539
ClinVar RCV Id: RCV000131729 RCV000487151 RCV001202065
ClinVar Variation Id: 922624
ClinVar RCV Id: RCV001182806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met234Ile
CA022513
NM_001258281.1:c.702G>A
CA346732941
NM_001258281.1:c.702G>C
CA346732942
NM_001258281.1:c.702G>T