Canonical Allele Identifier: PA645472624
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230546
ClinVar RCV Id: RCV000220130 RCV000411007 RCV000469366 RCV000589679 RCV003997848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp295Glu
CA041012
NM_000251.3:c.885C>G
CA346732909
NM_000251.3:c.885C>A