Canonical Allele Identifier: PA2826465400
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232707
ClinVar RCV Id: RCV000220420 RCV001053718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly695Val
CA10578002
NM_001258281.1:c.2084G>T