Canonical Allele Identifier: PA2826463157
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231094
ClinVar RCV Id: RCV000218499 RCV001857771
ClinVar Variation Id: 565518
ClinVar RCV Id: RCV000685101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg161Ser
CA10577944
NM_001258281.1:c.483A>C
CA346731861
NM_001258281.1:c.483A>T