Canonical Allele Identifier: PA2826465578
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1053073
ClinVar RCV Id: RCV001361367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr744Asn
CA346730256
NM_001258281.1:c.2231C>A