Canonical Allele Identifier: PA2826465501
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 801209
ClinVar RCV Id: RCV000985802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala725Pro
CA346730060
NM_001258281.1:c.2173G>C