Canonical Allele Identifier: PA891846897
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 575085
ClinVar RCV Id: RCV000697197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Trp117Leu
CA346730090
NM_000251.3:c.350G>T