Canonical Allele Identifier: PA2826464822
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753
ClinVar RCV Id: RCV000001823 RCV000076307 RCV000566777 RCV000630204 RCV002460877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro556Leu
CA019478
NM_001258281.1:c.1667C>T