Canonical Allele Identifier: PA294351
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142277
ClinVar RCV Id: RCV000131300 RCV000212579 RCV000545235 RCV003998100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg55Gly
CA018773
NM_000251.3:c.163C>G