Canonical Allele Identifier: PA357280
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220154
ClinVar RCV Id: RCV000203760 RCV000662969 RCV000771214 RCV001569238 RCV003997617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile169Met
CA039056
NM_000251.3:c.507A>G