Canonical Allele Identifier: PA645509929
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 439190
ClinVar RCV Id: RCV000508020 RCV000776722 RCV001539955 RCV002527341 RCV004003548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln718Glu
CA346729326
NM_000251.3:c.2152C>G