Canonical Allele Identifier: PA2826465096
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90874
ClinVar RCV Id: RCV000076376 RCV000491088 RCV000524375 RCV001284172 RCV001353848 RCV001804825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met622Arg
CA019937
NM_001258281.1:c.1865T>G