Canonical Allele Identifier: PA2579920255
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1785141
ClinVar RCV Id: RCV002421890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val686Leu
CA346729155
NM_000251.3:c.2056G>C
CA346729156
NM_000251.3:c.2056G>T