Canonical Allele Identifier: PA2826464984
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135856
ClinVar RCV Id: RCV000122984 RCV001013915 RCV003997406
ClinVar Variation Id: 1213458
ClinVar RCV Id: RCV001586659 RCV001882708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln596His
CA019664
NM_001258281.1:c.1788G>C
CA346728893
NM_001258281.1:c.1788G>T