Canonical Allele Identifier: PA2826465124
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 393457
ClinVar RCV Id: RCV000445396 RCV001014350 RCV003449101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Cys627Tyr
CA16609274
NM_001258281.1:c.1880G>A