Allele Registry

Canonical Allele Identifier: PA2826632570

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003484586

RCV004364854

ClinVar Variation:

2683985

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Glu721Gln	CA346756538 NM_001281493.2:c.2161G>C