Allele Registry

Canonical Allele Identifier: PA2826632856

Gene: MSH6 HGNC NCBI

ClinVar Allele:

405932

ClinVar RCV:

RCV000482150

RCV000560746

RCV000570886

RCV004003362

ClinVar Variation:

421879

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Pro784His	CA070513 NM_001281493.2:c.2351C>A