Canonical Allele Identifier: PA164986
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141281
ClinVar RCV Id: RCV000129729 RCV000460057 RCV000588274 RCV000761179 RCV002267870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile454Val
CA018091
NM_000251.3:c.1360A>G