Canonical Allele Identifier: PA658739450
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 491804
ClinVar RCV Id: RCV000584623 RCV000806010 RCV003465309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn792Ile
CA346730081
NM_000251.3:c.2375A>T