Allele Registry

Canonical Allele Identifier: PA645383668

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491655

RCV000504512

RCV000629920

RCV000759862

ClinVar Variation:

428337

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg1076Gly	CA070417 NM_000179.3:c.3226C>G