Canonical Allele Identifier: PA658672820
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455532
ClinVar RCV Id: RCV000547904 RCV000568306 RCV001572130 RCV002481753 RCV004003740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg631Lys
CA346728562
NM_000251.3:c.1892G>A