Canonical Allele Identifier: PA094859
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91105
ClinVar RCV Id: RCV000076608 RCV000491163 RCV000524412 RCV000662882 RCV000985811 RCV001194033 RCV004546430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly162Arg
CA021199
NM_000251.3:c.484G>A
CA346730616
NM_000251.3:c.484G>C