Canonical Allele Identifier: PA2826465048
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489930
ClinVar RCV Id: RCV000580145 RCV001764699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Tyr612Cys
CA346729119
NM_001258281.1:c.1835A>G