ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579911440
Gene: MSH2
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV002337803
RCV003108026
ClinVar Variation:
1743088
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000242.1:p.Gln160Glu
CA346730594
NM_000251.3:c.478C>G