Canonical Allele Identifier: PA331674
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91194
ClinVar RCV Id: RCV000235646 RCV000491084 RCV000630103 RCV002265598 RCV003389041 RCV003997180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys248Glu
CA022149
NM_000251.3:c.742A>G