Allele Registry

Canonical Allele Identifier: PA2826634829

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000570527

RCV000816280

RCV003465239

RCV004530607

ClinVar Variation:

483792

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Ala192Val	CA346746046 NM_001281494.2:c.575C>T