Canonical Allele Identifier: PA2826465024
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 439188
ClinVar RCV Id: RCV000508402 RCV001865650 RCV003159641 RCV004003547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met606Val
CA033352
NM_001258281.1:c.1816A>G