ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826465479
Gene: MSH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2453482
ClinVar RCV Id:
RCV003182937
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001245210.1:p.His719Asp
CA346729973
NM_001258281.1:c.2155C>G