Allele Registry

Canonical Allele Identifier: PA299455

Gene: MSH6 HGNC NCBI

ClinVar Allele:

180072

ClinVar RCV:

RCV000160678

RCV000212658

RCV000542696

RCV001174633

RCV003467252

ClinVar Variation:

182633

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser714Cys	CA009720 NM_000179.3:c.2141C>G