ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA336985
Gene: MSH2
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-3.7484091294
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000197107
RCV000491688
RCV001550881
RCV001798670
RCV003997022
ClinVar Variation:
216358
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000242.1:p.Lys909Arg
CA037327
NM_000251.3:c.2726A>G