Allele Registry

Canonical Allele Identifier: PA2826626281

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003595096

ClinVar Variation:

2710370

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly441Arg	CA068053 NM_001281492.2:c.1321G>C