Allele Registry

Canonical Allele Identifier: PA2826633114

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000206842

RCV000220316

RCV000482863

RCV001034622

ClinVar Variation:

220619

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Met842Arg	CA350840 NM_001281493.2:c.2525T>G