Allele Registry

Canonical Allele Identifier: PA645383804

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000220326

RCV000461508

RCV003422122

RCV003593509

ClinVar Variation:

230153

2741506

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly1105Arg	CA070646 NM_000179.3:c.3313G>A CA346758607 NM_000179.3:c.3313G>C