Canonical Allele Identifier: PA336688
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216342
ClinVar RCV Id: RCV000196756 RCV000214843 RCV000409612 RCV000586261 RCV003997013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg444Leu
CA027957
NM_000251.3:c.1331G>T