Canonical Allele Identifier: PA2826464243
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486884
ClinVar RCV Id: RCV000575075 RCV001302760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg416Thr
CA346726916
NM_001258281.1:c.1247G>C