Allele Registry

Canonical Allele Identifier: PA2826628448

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000132174

RCV000541079

RCV001174713

RCV001267890

RCV002514752

RCV003462035

ClinVar Variation:

142773

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly1027Cys	CA012982 NM_001281492.2:c.3079G>T