Canonical Allele Identifier: PA163839
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140888
ClinVar RCV Id: RCV000129124 RCV000210186 RCV000688403 RCV003477537
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn477His
CA018266
NM_000251.3:c.1429A>C