Allele Registry

Canonical Allele Identifier: PA916011373

Gene: MSH6 HGNC NCBI

ClinVar Allele:

180089

ClinVar RCV:

RCV000232219

RCV000562784

RCV000587626

RCV003488409

RCV003998502

ClinVar Variation:

182645

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Met944Val	CA012035 NM_001281492.2:c.2830A>G