Canonical Allele Identifier: PA658672391
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_000242.1:p.Thr456Ile
CA028117
NM_000251.3:c.1367C>T