Allele Registry

Canonical Allele Identifier: PA916011477

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000166804

RCV000701255

RCV003995533

ClinVar Variation:

187114

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Pro980Ser	CA012609 NM_001281492.2:c.2938C>T