Canonical Allele Identifier: PA2826465243
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1786935
ClinVar RCV Id: RCV002417908 RCV003121033 RCV004007401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly655Glu
CA346729348
NM_001258281.1:c.1964G>A