ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826464803
Gene: MSH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
653460
ClinVar RCV Id:
RCV000809239
RCV002406815
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001245210.1:p.Pro552Ser
CA346728431
NM_001258281.1:c.1654C>T