Allele Registry

Canonical Allele Identifier: PA2826631175

Gene: MSH6 HGNC NCBI

ClinVar Allele:

94722

ClinVar RCV:

RCV000822642

RCV001186406

RCV003450940

ClinVar Variation:

89248

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Cys392Arg	CA009656 NM_001281493.2:c.1174T>C