Canonical Allele Identifier: PA2826463721
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90516
ClinVar RCV Id: RCV000629705 RCV002408591 RCV003460713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu291Gln
CA017022
NM_001258281.1:c.871G>C