Canonical Allele Identifier: PA658671827
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455605
ClinVar RCV Id: RCV000529941 RCV001180426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys228Glu
CA040044
NM_000251.3:c.682A>G