ClinGen Allele Registry
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Canonical Allele Identifier:
PA094750
Gene: MSH2
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-4.0131639245
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000490598
RCV000491547
RCV001039917
ClinVar Variation:
427603
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000242.1:p.Asp660Gly
CA346728864
NM_000251.3:c.1979A>G