ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA294035
Gene: MSH2
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-2.7823488762
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000129363
RCV000212581
RCV000233259
RCV000662735
RCV003997495
ClinVar Variation:
141032
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000242.1:p.Ser87Cys
CA020808
NM_000251.3:c.260C>G