Canonical Allele Identifier: PA645474711
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418316
ClinVar RCV Id: RCV000485623 RCV001187838 RCV002280119 RCV003758780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp603His
CA16617590
NM_000251.3:c.1807G>C