Allele Registry

Canonical Allele Identifier: PA2826629347

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000074974

RCV000160701

RCV000202090

RCV000491705

RCV000542786

RCV000576708

RCV001355904

ClinVar Variation:

89506

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg1204Gln	CA015202 NM_001281492.2:c.3611G>A