Canonical Allele Identifier: PA331681
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91203
ClinVar RCV Id: RCV000539072 RCV001582562 RCV002408599 RCV003997182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met261Thr
CA022248
NM_000251.3:c.782T>C