Canonical Allele Identifier: PA2826463503
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91246
ClinVar RCV Id: RCV000076751 RCV000524912 RCV000567639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu244Arg
CA022554
NM_001258281.1:c.731T>G