Canonical Allele Identifier: PA2826465192
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408499
ClinVar RCV Id: RCV000469918 RCV000481613 RCV000491178 RCV004000781 RCV004533186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile642Val
CA034231
NM_001258281.1:c.1924A>G