Canonical Allele Identifier: PA2826465073
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90868
ClinVar RCV Id: RCV000076370 RCV000132039 RCV000202225 RCV000524373 RCV001264415 RCV001588897 RCV003452883
ClinVar Variation Id: 2673350
ClinVar RCV Id: RCV003455975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly617Arg
CA019900
NM_001258281.1:c.1849G>A
CA346729142
NM_001258281.1:c.1849G>C