ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645476058
Gene: MSH2
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-4.5367937147
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000486454
ClinVar Variation:
419367
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000242.1:p.Gln879Pro
CA16617609
NM_000251.3:c.2636A>C