Canonical Allele Identifier: PA2826463201
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2840193
ClinVar RCV Id: RCV003758430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Tyr172His
CA346732066
NM_001258281.1:c.514T>C