Canonical Allele Identifier: PA2826465424
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1356045
ClinVar RCV Id: RCV001880333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu702Gly
CA346729860
NM_001258281.1:c.2105A>G