Canonical Allele Identifier: PA1139677757
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 840218
ClinVar RCV Id: RCV001042160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser297Asn
CA346732920
NM_000251.3:c.890G>A