Allele Registry

Canonical Allele Identifier: PA645384475

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218152

RCV000570599

RCV000630095

RCV003998627

ClinVar Variation:

234558

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu1235Val	CA10577292 NM_000179.3:c.3703C>G