Canonical Allele Identifier: PA2826464813
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483736
ClinVar RCV Id: RCV000567575 RCV000806694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg555Pro
CA346728461
NM_001258281.1:c.1664G>C