Canonical Allele Identifier: PA2826463184
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1756711
ClinVar RCV Id: RCV002364858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr168Lys
CA346731989
NM_001258281.1:c.503C>A