Canonical Allele Identifier: PA2826463206
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1366704
ClinVar RCV Id: RCV001944808
ClinVar Variation Id: 3230854
ClinVar RCV Id: RCV004522968
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln173His
CA346732111
NM_001258281.1:c.519G>C
CA346732113
NM_001258281.1:c.519G>T