Canonical Allele Identifier: PA299351
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182576
ClinVar RCV Id: RCV000197978 RCV000217291 RCV000515278 RCV000590606 RCV000662843 RCV003330516 RCV003998481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu128Arg
CA021103
NM_000251.3:c.383T>G