Canonical Allele Identifier: PA645474953
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 422780
ClinVar RCV Id: RCV000482793 RCV000816301 RCV001013660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser637Cys
CA16617596
NM_000251.3:c.1910C>G