Canonical Allele Identifier: PA658671490
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455516
ClinVar RCV Id: RCV000525199 RCV001012654 RCV001260343 RCV003459177 RCV004003737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu56Gln
CA346728981
NM_000251.3:c.166G>C