Allele Registry

Canonical Allele Identifier: PA2826624890

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000132028

RCV000410426

RCV000464603

RCV000480539

RCV003153428

RCV003462027

RCV003998130

ClinVar Variation:

142675

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg113Cys	CA016337 NM_001281492.2:c.337C>T