Canonical Allele Identifier: PA2826465167
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428567
ClinVar RCV Id: RCV000491379 RCV001215708 RCV003449383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val636Glu
CA346729242
NM_001258281.1:c.1907T>A