Canonical Allele Identifier: PA2826462942
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91121
ClinVar RCV Id: RCV001353990 RCV002290960 RCV002336228 RCV001854331 RCV003997177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu107Pro
CA021269
NM_001258281.1:c.320T>C