Canonical Allele Identifier: PA2826465707
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182585
ClinVar RCV Id: RCV000160621 RCV000168241 RCV000656883 RCV000235176 RCV000663089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln780Arg
CA020697
NM_001258281.1:c.2339A>G