ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579924444
Gene: MSH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1796214
ClinVar RCV Id:
RCV002441588
RCV003102243
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000242.1:p.Thr934Ala
CA346732283
NM_000251.3:c.2800A>G