Canonical Allele Identifier: PA2826464783
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1447487
ClinVar RCV Id: RCV001996806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly548Arg
CA346728394
NM_001258281.1:c.1642G>A
CA346728395
NM_001258281.1:c.1642G>C