Canonical Allele Identifier: PA2826465671
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90991
ClinVar RCV Id: RCV000216575 RCV000479296 RCV000524391 RCV001357139 RCV003466966 RCV003997163
ClinVar Variation Id: 2587531
ClinVar RCV Id: RCV003377969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His773Gln
CA020666
NM_001258281.1:c.2319T>A
CA346730742
NM_001258281.1:c.2319T>G