Canonical Allele Identifier: PA2826464262
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90674
ClinVar RCV Id: RCV000076170 RCV000131869 RCV000411837 RCV000524343 RCV000590052 RCV001797621 RCV001798266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp421Glu
CA018356
NM_001258281.1:c.1263C>G
CA346727006
NM_001258281.1:c.1263C>A