Canonical Allele Identifier: PA2826463225
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408458
ClinVar RCV Id: RCV000570120 RCV000466771 RCV001821275 RCV001591088 RCV003463904 RCV004000774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg177Trp
CA040214
NM_001258281.1:c.529C>T