Canonical Allele Identifier: PA915984019
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483698
ClinVar RCV Id: RCV000574236
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly42Glu
CA346729711
NM_001258281.1:c.125G>A