Canonical Allele Identifier: PA169211
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142708
ClinVar RCV Id: RCV000132075 RCV000535324 RCV000503476 RCV000985801 RCV001353465 RCV003453090
ClinVar Variation Id: 2108540
ClinVar RCV Id: RCV003017672
ClinVar Variation Id: 3065347
ClinVar RCV Id: RCV003990424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly71Arg
CA020066
NM_000251.3:c.211G>C
CA346729065
NM_000251.3:c.211G>A
CA2580067374
NM_000251.3:c.210_211delinsCC