ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826463503
Gene: MSH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
91246
ClinVar RCV Id:
RCV000076751
RCV000524912
RCV000567639
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001245210.1:p.Leu244Arg
CA022554
NM_001258281.1:c.731T>G