Allele Registry

Canonical Allele Identifier: PA2826630657

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000223441

RCV000555846

RCV000564916

RCV000766399

RCV003469114

RCV003998645

ClinVar Variation:

234864

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Arg275Gly	CA068077 NM_001281493.2:c.823C>G