Canonical Allele Identifier: PA2826465201
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525729
ClinVar RCV Id: RCV000777516 RCV000629968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg645Leu
CA346729289
NM_001258281.1:c.1934G>T