Canonical Allele Identifier: PA2826465139
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90882
ClinVar RCV Id: RCV000076384 RCV002415564 RCV002228184 RCV004537293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Cys631Arg
CA019984
NM_001258281.1:c.1891T>C