Canonical Allele Identifier: PA645474782
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408524
ClinVar RCV Id: RCV000465743 RCV000483159 RCV000561447 RCV001192651 RCV003449133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg621Gly
CA031770
NM_000251.3:c.1861C>G