Canonical Allele Identifier: PA2826463452
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 245802
ClinVar RCV Id: RCV000236690 RCV000456430 RCV000563882 RCV003463695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser231Arg
CA10584210
NM_001258281.1:c.693C>G
CA346732917
NM_001258281.1:c.691A>C
CA346732923
NM_001258281.1:c.693C>A