Canonical Allele Identifier: PA2826464919
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_001245210.1:p.Ile582Asn
CA032124
NM_001258281.1:c.1745T>A