Canonical Allele Identifier: PA645471332
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232406
ClinVar RCV Id: RCV000215101 RCV000227027 RCV001030705 RCV001532987 RCV003997972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val89Ala
CA10577929
NM_000251.3:c.266T>C