Allele Registry

Canonical Allele Identifier: PA2826630522

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000479973

RCV000545794

RCV000574287

RCV000659891

RCV000765683

RCV003470532

RCV004002268

ClinVar Variation:

418743

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Lys243Glu	CA16617656 NM_001281493.2:c.727A>G