Canonical Allele Identifier: PA2826463633
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90504
ClinVar RCV Id: RCV000075999 RCV001250033 RCV002354266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly272Glu
CA016852
NM_001258281.1:c.815G>A