Allele Registry

Canonical Allele Identifier: PA2826633577

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000074918

RCV000129144

RCV000255857

RCV000524185

RCV001249986

RCV001532986

RCV002243694

RCV003460690

ClinVar Variation:

89450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Arg940del	CA013989 NM_001281493.2:c.2818_2820del