Allele Registry

Canonical Allele Identifier: PA167786

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000131212

RCV000477097

RCV002510790

RCV003998091

ClinVar Variation:

142218

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro199Leu	CA015926 NM_000179.3:c.596C>T