Canonical Allele Identifier: PA339117
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216341
ClinVar RCV Id: RCV000200127 RCV000564423 RCV000765666 RCV001589078 RCV003316110 RCV003155118 RCV003997012 RCV004528987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile418Met
CA027308
NM_000251.3:c.1254A>G