Allele Registry

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Canonical Allele Identifier: PA2826633321

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 846478

ClinVar RCV Id: RCV001049789

ClinVar Variation Id: 2986028

ClinVar RCV Id: RCV003843699

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ser886Arg	CA346760433 NM_001281493.2:c.2656A>C CA346760442 NM_001281493.2:c.2658T>A CA346760444 NM_001281493.2:c.2658T>G