Canonical Allele Identifier: PA645476302
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_000242.1:p.Met899Ile
CA10582028
NM_000251.3:c.2697G>T
CA346731621
NM_000251.3:c.2697G>A
CA346731622
NM_000251.3:c.2697G>C