Canonical Allele Identifier: PA2826463220
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 485845
ClinVar RCV Id: RCV000571179 RCV001319890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn176His
CA346732152
NM_001258281.1:c.526A>C