Canonical Allele Identifier: PA2826465542
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773619
ClinVar RCV Id: RCV003584475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His735Gln
CA346730194
NM_001258281.1:c.2205T>A
CA346730195
NM_001258281.1:c.2205T>G