Allele Registry

Canonical Allele Identifier: PA2826636769

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000131640

RCV000205918

RCV000212672

RCV000412088

RCV001356309

ClinVar Variation:

142495

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Asp641Tyr	CA010974 NM_001281494.2:c.1921G>T