Canonical Allele Identifier: PA2826465720
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134845
ClinVar RCV Id: RCV000121565 RCV000820212 RCV002221491 RCV002426668 RCV003997349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu783Val
CA020700
NM_001258281.1:c.2347C>G