Canonical Allele Identifier: PA2826464917
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016744
ClinVar RCV Id: RCV001315795 RCV002412012 RCV003462886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile582Thr
CA032140
NM_001258281.1:c.1745T>C