ClinGen Allele Registry
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Canonical Allele Identifier:
PA645475511
Gene: MSH2
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-5.0951645541
Linked Data - NCBI & NCI
ClinVar Allele:
244393
ClinVar RCV:
RCV000236064
RCV000556812
RCV000564620
RCV003469187
RCV003998917
ClinVar Variation:
246264
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000242.1:p.Asp742Asn
CA10584222
NM_000251.3:c.2224G>A