Canonical Allele Identifier: PA2826464145
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455485
ClinVar RCV Id: RCV000532242 RCV000562767 RCV004003732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr390Ile
CA028117
NM_001258281.1:c.1169C>T