ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA094996
Gene: MSH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
91044
ClinVar RCV Id:
RCV000076546
RCV002433581
RCV002465507
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000242.1:p.Leu93Phe
CA020925
NM_000251.3:c.277C>T