Canonical Allele Identifier: PA2826628758
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 638837
ClinVar RCV Id: RCV000791493 RCV002458409 RCV004001554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr1095Lys
CA071830
NM_001281492.2:c.3284C>A