Canonical Allele Identifier: PA2826463723
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141266
ClinVar RCV Id: RCV000129706 RCV001065111 RCV003997517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu291Asp
CA017034
NM_001258281.1:c.873G>C
CA346733271
NM_001258281.1:c.873G>T