Canonical Allele Identifier: PA2826636684
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483880
ClinVar RCV Id: RCV000574967 RCV001356005 RCV001853720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys621Arg
CA346755454
NM_001281494.2:c.1862A>G