Canonical Allele Identifier: PA2826465731
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127638
ClinVar RCV Id: RCV000115520 RCV000196855 RCV000221197 RCV003997274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu786Gln
CA020723
NM_001258281.1:c.2356G>C