Canonical Allele Identifier: PA2826463807
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237358
ClinVar RCV Id: RCV000229489 RCV000479748 RCV000662583 RCV001017396 RCV001193852 RCV003491996 RCV003998751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln311Arg
CA027052
NM_001258281.1:c.932A>G