Canonical Allele Identifier: PA645474223
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 265366
ClinVar RCV Id: RCV000255442 RCV000704303 RCV001010317 RCV002248492 RCV003995743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln402Glu
CA10588342
NM_000251.3:c.1204C>G