Canonical Allele Identifier: PA645472625
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232681
ClinVar RCV Id: RCV000214812 RCV000659880 RCV001067169 RCV003997995
ClinVar Variation Id: 1312637
ClinVar RCV Id: RCV001763643 RCV003163879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe296Leu
CA10577958
NM_000251.3:c.888C>G
CA346732911
NM_000251.3:c.886T>C
CA346732916
NM_000251.3:c.888C>A