Canonical Allele Identifier: PA2826464292
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408512
ClinVar RCV Id: RCV000458190 RCV000570881 RCV003470448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu430Ser
CA16610877
NM_001258281.1:c.1289T>C