ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826465201
Gene: MSH2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
518447
ClinVar RCV:
RCV000629968
RCV000777516
ClinVar Variation:
525729
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001245210.1:p.Arg645Leu
CA346729289
NM_001258281.1:c.1934G>T