ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA331681
Gene: MSH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
91203
ClinVar RCV Id:
RCV000539072
RCV001582562
RCV002408599
RCV003997182
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000242.1:p.Met261Thr
CA022248
NM_000251.3:c.782T>C