ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826465124
Gene: MSH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
393457
ClinVar RCV Id:
RCV000445396
RCV001014350
RCV003449101
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001245210.1:p.Cys627Tyr
CA16609274
NM_001258281.1:c.1880G>A