Canonical Allele Identifier: PA915984271
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1741885
ClinVar RCV Id: RCV002342452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala88Pro
CA346730516
NM_001258281.1:c.262G>C