Canonical Allele Identifier: PA2826464164
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 485825
ClinVar RCV Id: RCV000567509 RCV000685208 RCV000759100 RCV003459384 RCV004001116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met394Thr
CA346724826
NM_001258281.1:c.1181T>C