Canonical Allele Identifier: PA915984334
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_001245210.1:p.Gly96Arg
CA021199
NM_001258281.1:c.286G>A
CA346730616
NM_001258281.1:c.286G>C