Allele Registry

Canonical Allele Identifier: PA645380544

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000479973

RCV000545794

RCV000574287

RCV000659891

RCV000765683

RCV003470532

RCV004002268

ClinVar Variation:

418743

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Lys545Glu	CA16617656 NM_000179.3:c.1633A>G