Canonical Allele Identifier: PA2826464764
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 419452
ClinVar RCV Id: RCV000479405 RCV001186882 RCV001851163
ClinVar Variation Id: 925536
ClinVar RCV Id: RCV001187513 RCV002559130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His544Gln
CA16617592
NM_001258281.1:c.1632C>G
CA346728371
NM_001258281.1:c.1632C>A