ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579922627
Gene: MSH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2820361
ClinVar RCV Id:
RCV003760993
RCV004371706
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000242.1:p.Phe826Ser
CA346730589
NM_000251.3:c.2477T>C