Canonical Allele Identifier: PA2826464998
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 233706
ClinVar RCV Id: RCV000217308 RCV001301645 RCV003462530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile601Val
CA10577992
NM_001258281.1:c.1801A>G