Canonical Allele Identifier: PA645474637
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 427602
ClinVar RCV Id: RCV000490580 RCV001856915 RCV002404286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu556Trp
CA346728044
NM_000251.3:c.1667T>G