Canonical Allele Identifier: PA331373
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90771
ClinVar RCV Id: RCV000076270 RCV000700587 RCV002408594 RCV003452855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly587Arg
CA019199
NM_000251.3:c.1759G>C