Canonical Allele Identifier: PA645471942
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237404
ClinVar RCV Id: RCV000227866 RCV000235996 RCV001026208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn242Ser
CA040185
NM_000251.3:c.725A>G