Canonical Allele Identifier: PA2826465928
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237391
ClinVar RCV Id: RCV000233718 RCV001016339 RCV001262889 RCV003469138 RCV003998762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met833Ile
CA10582028
NM_001258281.1:c.2499G>T
CA346731621
NM_001258281.1:c.2499G>A
CA346731622
NM_001258281.1:c.2499G>C