Allele Registry

Canonical Allele Identifier: PA2826637469

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000220326

RCV000461508

RCV003422122

RCV003593509

ClinVar Variation:

230153

2741506

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gly803Arg	CA070646 NM_001281494.2:c.2407G>A CA346758607 NM_001281494.2:c.2407G>C