Canonical Allele Identifier: PA658671879
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479797
ClinVar RCV Id: RCV000569886 RCV001865717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly250Arg
CA346732311
NM_000251.3:c.748G>A
CA346732314
NM_000251.3:c.748G>C