Canonical Allele Identifier: PA2826465418
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186151
ClinVar RCV Id: RCV000165690 RCV000202197 RCV000766654 RCV000798203 RCV003462184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile700Val
CA020456
NM_001258281.1:c.2098A>G