Canonical Allele Identifier: PA891844674
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 584609
ClinVar RCV Id: RCV000708839 RCV001014077 RCV001064045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn671Ser
CA346729083
NM_000251.3:c.2012A>G