Allele Registry

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Canonical Allele Identifier: PA916011028

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 819786

ClinVar RCV Id: RCV001012653

ClinVar Variation Id: 819787

ClinVar RCV Id: RCV001012655

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly56Arg	CA346734981 NM_001281492.2:c.166G>A CA346734982 NM_001281492.2:c.166G>C