Canonical Allele Identifier: PA2579911429
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825181
ClinVar RCV Id: RCV001023066 RCV003320786 RCV004004634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln160Arg
CA346730598
NM_000251.3:c.479A>G