Canonical Allele Identifier: PA2573061935
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1332149
ClinVar RCV Id: RCV001804665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn596Lys
CA46700072
NM_000251.3:c.1788T>A
CA346728303
NM_000251.3:c.1788T>G