Allele Registry

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Canonical Allele Identifier: PA2826625782

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 571875

ClinVar RCV Id: RCV000693125 RCV001187695

ClinVar Variation Id: 818962

ClinVar RCV Id: RCV001011091

ClinVar Variation Id: 2869887

ClinVar RCV Id: RCV003759433

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Phe321Leu	CA346744665 NM_001281492.2:c.961T>C CA346744681 NM_001281492.2:c.963C>A CA346744688 NM_001281492.2:c.963C>G