Canonical Allele Identifier: PA2826465673
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1722340
ClinVar RCV Id: RCV002302454 RCV002427774 RCV003098017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His773Tyr
CA346730733
NM_001258281.1:c.2317C>T