Canonical Allele Identifier: PA915966684
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 641572
ClinVar RCV Id: RCV000794839 RCV001010432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly410_Gln413del
CA915943903
NM_000251.3:c.1227_1238del