Canonical Allele Identifier: PA2579910565
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 957030
ClinVar RCV Id: RCV001229939 RCV001355866 RCV001760227 RCV002322108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala111Val
CA346730012
NM_000251.3:c.332C>T