ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826465117
Gene: MSH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
265620
ClinVar RCV Id:
RCV000255143
RCV000501019
RCV000772137
RCV000803818
RCV001353568
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001245210.1:p.Gly626Glu
CA10588345
NM_001258281.1:c.1877G>A