Canonical Allele Identifier: PA2826462882
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2100425
ClinVar RCV Id: RCV003025886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Trp51Arg
CA346730086
NM_001258281.1:c.151T>A
CA346730087
NM_001258281.1:c.151T>C