Canonical Allele Identifier: PA2826465925
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 480886
ClinVar RCV Id: RCV000569579 RCV000629815 RCV003222042 RCV004000905 RCV003987605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu832Asp
CA46712554
NM_001258281.1:c.2496A>C
CA346731601
NM_001258281.1:c.2496A>T