Canonical Allele Identifier: PA2826462933
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428533
ClinVar RCV Id: RCV000491118 RCV001053469 RCV001532970 RCV000985813 RCV004003472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln104Arg
CA346730701
NM_001258281.1:c.311A>G