Allele Registry

Canonical Allele Identifier: PA916011933

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000132174

RCV000541079

RCV001174713

RCV001267890

RCV002514752

RCV003462035

ClinVar Variation:

142773

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Gly855Cys	CA012982 NM_001281494.2:c.2563G>T