Canonical Allele Identifier: PA2826627673
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 645219
ClinVar RCV Id: RCV000799261 RCV002487680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr765Arg
CA069436
NM_001281492.2:c.2294C>G