Canonical Allele Identifier: PA1139677307
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 925305
ClinVar RCV Id: RCV001187160 RCV002560905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg227Gly
CA040008
NM_000251.3:c.679A>G