Canonical Allele Identifier: PA2826626940
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479899
ClinVar RCV Id: RCV000570519 RCV000802427 RCV004000872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr590Ile
CA068511
NM_001281492.2:c.1769C>T