Canonical Allele Identifier: PA2826465550
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455562
ClinVar RCV Id: RCV000543029 RCV000588000 RCV001015432 RCV001030715 RCV004003747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr737Ala
CA46705221
NM_001258281.1:c.2209A>G