ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA187370
Gene: MSH2
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-2.8325107619
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000163067
RCV000168408
RCV000662475
RCV000759104
RCV001804892
RCV003995232
ClinVar Variation:
183977
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000242.1:p.Ile633Val
CA019526
NM_000251.3:c.1897A>G