Allele Registry

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Canonical Allele Identifier: PA2826628873

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 188262

ClinVar RCV Id: RCV000168238 RCV000214013 RCV000484522 RCV000662602 RCV000780480 RCV003462260 RCV003491921 RCV003995615

ClinVar Variation Id: 2773666

ClinVar RCV Id: RCV003585639

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Thr1117Ser	CA014131 NM_001281492.2:c.3350C>G CA346761053 NM_001281492.2:c.3349A>T