Canonical Allele Identifier: PA2579920835
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2064560
ClinVar RCV Id: RCV002953513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly721Arg
CA346729346
NM_000251.3:c.2161G>A
CA346729347
NM_000251.3:c.2161G>C