Canonical Allele Identifier: PA2826464906
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90822
ClinVar RCV Id: RCV000115513 RCV000540956 RCV000573883 RCV000662923 RCV003997155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln579Glu
CA019587
NM_001258281.1:c.1735C>G