Canonical Allele Identifier: PA645474977
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 234021
ClinVar RCV Id: RCV000222363 RCV000523371 RCV000629936 RCV001355204 RCV003469093 RCV003998593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile648Asn
CA032124
NM_000251.3:c.1943T>A