ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826463650
Gene: MSH2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000076002
RCV001213427
ClinVar Variation:
90507
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001245210.1:p.Leu275Pro
CA016875
NM_001258281.1:c.824T>C