Allele Registry

Canonical Allele Identifier: PA2826634832

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000772563

RCV001766602

RCV001856021

RCV003999973

ClinVar Variation:

628220

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg193Gln	CA346746059 NM_001281494.2:c.578G>A