Canonical Allele Identifier: PA2579919628
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1783071
ClinVar RCV Id: RCV002413198 RCV003594280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile648Val
CA46700513
NM_000251.3:c.1942A>G