Canonical Allele Identifier: PA658673204
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_000242.1:p.Glu898Asp
CA46712554
NM_000251.3:c.2694A>C
CA346731601
NM_000251.3:c.2694A>T