Allele Registry

Canonical Allele Identifier: PA210825

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000074918

RCV000129144

RCV000255857

RCV000524185

RCV001249986

RCV001532986

RCV002243694

RCV003460690

ClinVar Variation:

89450

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg1242del	CA013989 NM_000179.3:c.3724_3726del