Allele Registry

Canonical Allele Identifier: PA2826633540

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218152

RCV000570599

RCV000630095

RCV003998627

ClinVar Variation:

234558

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Leu933Val	CA10577292 NM_001281493.2:c.2797C>G