Canonical Allele Identifier: PA2826463160
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_001245210.1:p.Lys162Glu
CA040044
NM_001258281.1:c.484A>G