Canonical Allele Identifier: PA645474377
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408482
ClinVar RCV Id: RCV000458047 RCV000573378 RCV003463907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln493Leu
CA028775
NM_000251.3:c.1478A>T