Canonical Allele Identifier: PA197017
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 187208
ClinVar RCV Id: RCV000166913 RCV000484021 RCV001058479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro895Arg
CA020884
NM_000251.3:c.2684C>G