Canonical Allele Identifier: PA645471165
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408464
ClinVar RCV Id: RCV000561205 RCV000662999 RCV000470501 RCV001284007 RCV004000777
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala50Gly
CA16610845
NM_000251.3:c.149C>G